WO2003053669A1 - Textured surface having undercut micro recesses in a surface - Google Patents

Textured surface having undercut micro recesses in a surface Download PDF

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Publication number
WO2003053669A1
WO2003053669A1 PCT/US2002/039743 US0239743W WO03053669A1 WO 2003053669 A1 WO2003053669 A1 WO 2003053669A1 US 0239743 W US0239743 W US 0239743W WO 03053669 A1 WO03053669 A1 WO 03053669A1
Authority
WO
WIPO (PCT)
Prior art keywords
implant
bone
ellipsoid
textured
datum
Prior art date
Application number
PCT/US2002/039743
Other languages
French (fr)
Inventor
Mark Amrich
Jonathan L. Rolfe
Joseph Buturlia
Robert F. Lynch
Original Assignee
Tecomet, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tecomet, Inc. filed Critical Tecomet, Inc.
Priority to EP02792362A priority Critical patent/EP1463630A1/en
Priority to JP2003554419A priority patent/JP2005512702A/en
Priority to AU2002357821A priority patent/AU2002357821A1/en
Priority to CA002470068A priority patent/CA2470068A1/en
Priority to MXPA04005702A priority patent/MXPA04005702A/en
Publication of WO2003053669A1 publication Critical patent/WO2003053669A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/02Local etching
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/80Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates
    • A61B17/8085Cortical plates, i.e. bone plates; Instruments for holding or positioning cortical plates, or for compressing bones attached to cortical plates with pliable or malleable elements or having a mesh-like structure, e.g. small strips
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/4455Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages
    • A61F2/446Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages having a circular or elliptical cross-section substantially parallel to the axis of the spine, e.g. cylinders or frustocones
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B3/00Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form
    • B32B3/26Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • B32B3/30Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by a layer formed with recesses or projections, e.g. hollows, grooves, protuberances, ribs
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C8/00Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools
    • A61C8/0018Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the shape
    • A61C8/0037Details of the shape
    • A61C2008/0046Textured surface, e.g. roughness, microstructure
    • AHUMAN NECESSITIES
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    • A61CDENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
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    • A61C8/0012Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy
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    • A61F2/02Prostheses implantable into the body
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    • A61F2/02Prostheses implantable into the body
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
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Definitions

  • the invention relates to the production of textured surfaces for medical, industrial, and commercial applications and is directed more particularly to surfaces having undercut micro recesses.
  • the femoral sub-assembly in an artificial hip, including a femoral sub-assembly for positioning in a patient's femur, and an acetabular sub-assembly for positioning in the patient's acetabulum, the femoral sub-assembly includes an artificial stem which is typically provided with a textured surface, and the acetabular sub-assembly includes an acetabular cup which is typically provided with a textured surface, the textured surfaces being provided to promote bone in-growth.
  • one known method is to provide a mass of titanium spheres vacuum fused onto the datum surface of the implant. This method is described in U.S. Patent No. 4,834,756, issued May 30, 1989, to Robert V. Kenna. In a similar procedure, described in U.S. Patent No. 4,644,942, issued February 24, 1987 to Kenneth R. Sump, an extractable component and titanium spheres are densified as a coating, which is fused onto a datum surface of the implant, and the extractable component subsequently is extracted. While an improvement over untreated metal, questions have arisen over the longevity of usefulness of the implanted devices utilizing such surfaces. It is questionable whether there is substantial genuine adhesion.
  • An acetabular cup is a hemispherical device that is implanted in the acetabulum in hip-replacement surgery.
  • the cup serves as a "socket" in a ball-and-socket joint of the hip.
  • a lining in the cup consists of a biologically inert anti-friction bearing surface, such as high molecular weight polyethylene.
  • the external portion of the cup is usually made of a biocompatible metal, such as cobalt-chromium or titanium alloys that have the stiffness needed to support the bearing surface, and the dimensional stability needed to prevent deflection or displacement of the bond formed to the surface of the host bone.
  • a strong mechanical bond to the bone is needed because, in use, the joint is subjected to strong mechanical forces.
  • the exterior of the cup is textured by diffusion bonding metal spheres so as to form a complex network on the exterior surface, in hopes that bone ingrowth will generate a mechanical bond.
  • Some manufacturers machine patterns of grooves in these surfaces. Because of metallurgical annealing in the fusion process, and limitations in machining, the surfaces so generated have not been optimal and have not reached the desired installed-life duration. When the cup is installed, an accompanying reamer is furnished to machine the bone surface to close dimensional fit to the replacement device.
  • an acetabular implant having an improved exterior surface that effects a short-term bond with the bone to which the implant is affixed, and that provides for long-term increased bonding between the implant and the bone, and that further requires no reamer or other bone-machining device.
  • a preferred embodiment of the invention is a textured surface which is adapted to interlock with an adjacent body and method of producing a textured surface.
  • a further embodiment is to provide a texture having an undercut micro recesses in a surface of a body and method of producing a textured surface.
  • a still further embodiment provides recesses in a desired pattern which is measurable and predictable, and which can be duplicated and repeated precisely in any selected number of surfaces and method of producing a textured surface.
  • a still further embodiment is a surgical implant device wherein the material of the device retains its metallurgical properties throughout production and method of producing a textured surface.
  • a still further embodiment is a surgical implant, with a textured surface that promotes the in-growth of tissue and/or bone to securely interconnect the implant and the tissue and/or bone and method of producing a textured surface.
  • a still further object is to provide an implant with surfaces that include undercut and interconnecting recesses which promote and facilitate ingrowth of bone and which, upon implantation, facilitate a "scratch fit" with bone, to stabilize the position of the surface on the bone and to initiate an interconnection process between the implant and the bone.
  • the "scratch fit” is accomplished by the textured surface scraping bone from the implant site during a press fit implantation, thereby producing autografted bone in the voids of the textured surface.
  • a still further embodiment is a surgical implant for attachment to tissue (e.g., bone).
  • tissue e.g., bone
  • a still further embodiment is a surgical implant for attachment to bone.
  • a still further embodiment is a surgical implant facilitating bone harvesting and seeding of the surgical implant with particulate bone matter during attachment of the implant to the bone.
  • a still further embodiment is a surgical implant which exhibits a precise fit with a bone implant site, to reduce micro-motion between the implant and the bone site.
  • a still further embodiment of the invention is to provide a surgical implant having undercut micro recesses with sharply defined edges in a bone-engaging surface thereof.
  • Yet another embodiment of the invention is the provision of an article, having a surface that includes a multiplicity of undercut microrecesses in the surface, such that the article thereby exhibits a greater fractal area at a level below the surface than is exhibited at the surface, the article produced by a method comprising the steps of applying a maskant layer to substantially an entirety of the article surface, removing the maskant layer in selected loci to expose underlying portions of the article surface in a selected, predictable, and reproducible pattern, applying an etchant to the exposed underlying surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce a multiplicity of undercut recesses, and removing the remaining maskant layer portions to provide the article surface in exposed condition with the multiplicity of recesses undercut and comprising interconnected recesses, to provide an engineered pattern of the recesses.
  • a surgical implant having facility for stimulating ingrowth of bone upon attachment of the implant to a bone that is produced by a method that includes the steps of: providing a rigid article; applying a maskant layer to substantially an entirety of a datum surface of the article; removing portions of the maskant layer in selected loci to expose underlying portions of the surface of the article; applying an etchant to the exposed underlying surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce a multiplicity of undercut recesses having sharp edges at their intersections with the datum surface; and removing the remaining portions of the maskant layer to provide the datum surface in exposed condition with the sharp edges for shaving particulate matter from the bone, and with the recesses for receiving and retaining the bone particulate matter for stimulating ingrowth of bone.
  • a textured surface in a surgical implant produced by a method that includes the steps of: applying a maskant layer to substantially an entirety of a datum surface of the implant; removing portions of the maskant layer in selected loci to expose underlying portions of the datum surface of the implant; applying an etchant to the exposed underlying datum surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce a multiplicity of undercut recesses having sharp edges at their intersections with the datum surface; and removing the remaining portions of the maskant layer to provide the datum surface in exposed condition with the sharp edges for shaving particulate matter from the bone, and with the recesses for receiving and retaining the bone particulate matter for stimulating in-growth of bone.
  • a surgical implant that is attached to a bone, in accordance with a method comprising the steps of: providing a surgical implant having a datum surface, a multiplicity of micro recesses in the datum surface, and bone milling structure on the datum surface; pressing the datum surface against a surface of the bone; and urging the implant along the bone surface to mill particulate bone matter from the bone, wherein the recesses receive and retain the particulate bone matter to stimulate ingrowth of the bone into the datum surface.
  • a surgical implant having a datum surface and a multiplicity of undercut microrecesses in the datum surface, such that the implant exhibits a greater fractal area at the level below the datum surface than is exhibited at the datum surface, intersections of the datum surface and the recesses defining sharp edges; pressing the datum surface against a surface of the bone, and urging the implant along the bone surface, to cause the sharp edges to shave particulate bone matter from the bone, wherein the recesses receive and retain the particulate bone matter to stimulate ingrowth of the bone to attach the surgical implant to the bone.
  • a method for bone harvesting and seeding of a surgical implant with particulate bone matter during attachment of the implant to the bone comprising the steps of providing a surgical implant having a surface for engagement with a bone surface, the implant having a multiplicity of undercut micro recesses and bone milling structure in the surface thereof, wherein moving the implant along the bone, such that the milling structure dislocates particulate bone matter from the bone, the bone matter falling into the micro recesses and retained thereby to stimulate ingrowth of the bone into the undercut recesses harvests the bone and seeds the surgical implant with particulate bone matter during attachment of the implant to the bone.
  • a surgical implant having generally opposed datum surfaces spaced from each other by a predetermined distance, each of the datum surfaces being adapted to interlock with a bone surface that is made by a process comprising the steps of providing an article having first and second datum surface portions adapted to respectively engage first and second bone surfaces, the datum surface portions being spaced from each other by the predetermined distance which is substantially equal to a distance between the first and second bone surfaces; applying a maskant layer to substantially an entirety of each of the datum surfaces; removing the maskant layers in selected loci to expose underlying portions of the datum surfaces in a selected pattern; applying an etchant to the exposed underlying datum surface portions for a time sufficient to etch the exposed portions of the datum surfaces and to enable the etchant to etch beneath the remaining maskant layers and produce undercut recesses; and removing the remaining maskant to provide the opposed datum surfaces in exposed condition with the multiplicity of undercut recesses and devoid of structure protrud
  • a surgical implant comprising an article having a datum surface for abutting engagement with a bone, and a multiplicity of undercut micro recesses in the datum surface, such that the body exhibits a greater fractal area at a level below the surface than is exhibited at the surface.
  • Intersections of the recesses and the datum surface define sharp edges adapted to cut the bone and produce bone particulates.
  • the recesses are adapted to receive and retain the bone particulates cut from the bone by the edges, to stimulate ingrowth of the bone into the recesses.
  • a further object of the invention is, therefore, to provide an acetabular cup having an outer bone-engaging surface provided with a multiplicity of sharp-edged undercut recesses for receiving bone particulates milled from the bone by the sharp edges during the mounting
  • a further object of the invention is to provide a method for attaching such acetabular cup to a host bone.
  • a feature of the invention is the provision of an acetabular implant having a datum surface for abutting engagement with a bone, and a multiplicity of undercut micro recesses in the datum surface, such that the body exhibits a greater fractal area at a level below the surface than is exhibited at the surface. Intersections of the recesses and the datum surface define sharp edges adapted to cut the bone and produce bone particulates. The recesses are adapted to receive and retain the bone particulates cut from the bone by the edges, to stimulate ingrowth of the bone into the recesses.
  • a method for attaching an acetabular orthopedic surgical implant to a host bone comprises providing an acetabular cup having a datum surface, a multiplicity of micro recesses in the datum surface, and a bone-milling structure on the datum surface, pressing the datum surface against a surface of the host bone, and urging the implant along the host-bone surface to ream the host bone and to mill particulate bone matter, from the host bone.
  • the recesses are adapted to receive and retain the particulate bone matter which stimulates ingrowth of the host bone.
  • FIG. 1 is a diagrammatic sectional view of an article having a surface in which it is desired to provide a multiplicity of undercut micro recesses;
  • FIG. 2 depicts the article of FIG. 1 with a layer of maskant material deposited on the aforesaid surface;
  • FIG. 3 depicts the article and maskant layer of FIG. 2 with the maskant layer in part removed;
  • FIG. 4 is similar to FIG. 3 and showing portions of the article not covered by maskant etched away to provide undercut and interconnected recesses;
  • FIG. 5 is similar to FIG. 4, but showing the remaining maskant layer stripped away;
  • FIGs. 6-10 are progressive diagrammatic sectional views showing positioning of the article adjacent a bone and interconnection of the article and the bone;
  • FIG. 11 is a diagrammatic sectional view of a surgical implant having a plurality of surfaces treated as illustrated in FIGS. 2-10;
  • FIG 12 is a diagrammatic sectional view of structural features of the a surface texture;
  • FIG 13 is a three-dimensional illustration of a textured pattern
  • FIG 14 is a diagrammatic sectional view of a complex ellipsoid
  • FIGs. 15a- 15c illustrate diagrammatic sectional views off structural features of a textured surface
  • FIG. 16 is a diagrammatic sectional view of a complex ellipsoid
  • FIG. 16A is a diagrammatic sectional view showing an embodiment of complex ellipsoids with an oblique orientation
  • FIG. 16B illustrates an exemplary textured structure
  • FIG. 16C - 16D are diagrammatic sectional views of a textured structure being inserted into a bone channel
  • FIGs. 17A - 17E are three-dimensional illustrations of exemplary textures
  • FIGs. 18 - 27 are diagrammatic cross-sectional views of successive stages in the making of a mesh-and-plate implant in accordance with an embodiment of the invention
  • FIG. 28 is a top plan view of a mesh-and-plate implant made in accordance with the method illustrated in FIGs. 18-27;
  • FIG. 29 is similar to FIG. 28, but illustrative of an alternative implant;
  • FIG. 30 is an enlarged illustration of the mesh portions of the implants of FIGs. 28 and 29;
  • FIG. 31 is a three-dimensional illustration of a textured implant
  • FIG. 32 is a diagrammatic cross-section of an implant
  • FIG. 33 is an illustration of an implant with protrusions
  • FIG. 34 is a diagrammatic cross-sectional view of an implant with protrusions
  • FIG. 35 is a diagrammatic cross sectional view of a textured implant
  • FIG. 36 is a diagrammatic cross sectional view of an implant with recesses
  • FIGs. 37A-37C illustrate implants with apertures;
  • FIGs. 38A-38D illustrate implants with ribs
  • FIGs. 39A - 39C are diagrammatic cross-sections illustrating textured implants
  • FIG. 40 illustrates a two dimensional pattern of the present invention
  • FIG. 41 is a diagrammatic illustration of a barbed implant
  • FIG. 42 A is a diagrammatic cross-sectional illustration of an implant having a directionally impinged textured surface
  • FIG. 42B is a diagrammatic cross-sectional illustration of an implant having a non- directionally impinged textured surface.
  • FIG. 43 is a side elevational view of a hip replacement assembly, including an acetabular cup illustrative of an embodiment of the invention.
  • FIG. 44 is an exploded perspective view of the assembly of FIG. 43;
  • FIGS. 45-49 are progressive diagrammatic sectional views illustrating a method for making an acetabular cup datum surface having undercut micro recesses;
  • FIGS. 50-54 are progressive diagrammatic sectional views showing positioning of the acetabular cup adjacent a bone, reaming of the bone, and interconnection of the cup and the bone.
  • Undercutting occurs, for example, when the chemical etchant removes metal beyond the boundary of a maskant, or resist layer. Often, such undercutting limits the fine resolution needed for many processes, such as the production of electronic devices, rotogravure plates, and other fine parts.
  • predetermined and controlled undercutting may be exploited and utilized to produce useful and novel three-dimensional geometries by allowing the undercutting effect to expand deeper regions of a chemically applied pattern, so that the resulting treatment layer is an engineered pattern of undercut recesses. This provides sharp geometries when desired, and produces a higher void volume and larger fractal dimensions than are obtainable by other methods.
  • the metal of the complex pattern is identical and contiguous with the base metal of the treated body, because it is generated in the body, and not later applied, such as the fused metal spheres mentioned hereinabove.
  • nick-bend failures or "notch failures."
  • An example of a notch failure is crack propagation in metal surfaces. Such propagation is known to occur, for example, in materials having an applied surface texture.
  • An example of a testing method for the measurement of creep crack growth rates in metals is provided in ASTM Standard El 457- 00, which is herein incorporated by reference in its entirety.
  • One material that is particularly suited for implant applications is titanium. The susceptibility of titanium to crack propagation is well documented. Annealing is one method to relieve strain from a material surface such as titanium. Annealing, however, can have other deleterious effects on metals (e.g., increased softness).
  • Another documented method for mitigating nick-bend failures is to strain relieve the material by, for example, removing the "rind", "skin" or outer surface of the metal that has been strained.
  • techniques for removing rind includes machining, grinding, laser welding or laser machining involving thermal shock and sudden phase changes. These techniques may be employed to expose the pristine metal beneath the surface. In some cases, however, removing the rind from a textured surface has the unwanted effect of removing a portion of the texture.
  • lasers are used to machine a metal (e.g., applying a texture to a surface using laser etching techniques)
  • there is created an area of increased strain where the laser acted upon the surface of the material.
  • One technique for strain release of that affected area is to remove the surface of the material. Where laser machining was performed for the purpose of applying a texture, removing that affected area would, in some cases, reduce or eliminate the effectiveness of the texture.
  • the methods and products of the present invention avoid this problem.
  • those effects are minimized or eliminated during the etching process resulting in a strain-reduced/relieved textured surface. That is, the strained regions of the surface are etched-away to relieve the strain, without forming a non-strained region.
  • strained metal such as where a laser has been applied to a surface
  • the laser ablation of maskant e.g., to expose the surface of the metal for later etching
  • increases localized strain on the surface of the metal thereby focusing future etching to produce a precisely textured strain-relieved surface.
  • the strained areas etch somewhat more quickly thereby promoting the preferentially accelerated resolution of these strains.
  • the textures described herein are useful in the medical, industrial, consumer product, computer, electrical, and mechanical fields.
  • textures are useful in orthopeadic implants (e.g., in artificial hips, knees, acetabular cups, ankles, shoulders, and interbody fusion devices); spinal implants (e.g., spinal fusion devices, articulating intravertebrae devices, and external spinal fixation devices); neurocranial and maxillofacial implants (e.g., fracture plates and mesh, scafolds, and bridges); dental implants (e.g., osseointegration posts); joint replacement implants, cemented and cementless applications, and any medically implanted device where there is a need for improved fixation.
  • orthopeadic implants e.g., in artificial hips, knees, acetabular cups, ankles, shoulders, and interbody fusion devices
  • spinal implants e.g., spinal fusion devices, articulating intravertebrae devices, and external spinal fixation devices
  • neurocranial and maxillofacial implants
  • Such improved fixation is useful between metal to tissue (e.g., bone), metal to plastic, metal to adhesive, soft tissue to bone, ligament to bone, soft tissue to implant, positional stability of implant (e.g., rough surface to hold implant in place during a surgical procedure) and for providing increased vascular flow (e.g., textured surface provides space between the implant and bone to allow for greater vascular flow between bone and implant).
  • metal to tissue e.g., bone
  • metal to plastic e.g., metal to plastic, metal to adhesive, soft tissue to bone, ligament to bone, soft tissue to implant, positional stability of implant (e.g., rough surface to hold implant in place during a surgical procedure) and for providing increased vascular flow (e.g., textured surface provides space between the implant and bone to allow for greater vascular flow between bone and implant).
  • textures have use in any component device in which a material requires a surface conditioning to promote adhesion or increase friction.
  • exemplary fields include aerospace (e.g., fusilage bonding and fasteners); automotive (e.g., brake shoes to brake pads), sports gloves (e.g., rock climbing, football and golf gloves), composites (e.g., golf club heads, and any other contact surfaces where increased grip is desired), and tool sharpening.
  • Other applications in industry and manufacturing will be apparent for the textured pattern of the present invention, including cutting surfaces (e.g., rasps, dental drills, medical files, burrs and orthopeadic cutters). Further utility will be found where improved adhesion is desired (e.g., metal to metal adhesion, polymer to polymer adhesion, metal to polymer adhesion, and on layers of material that are laminated to one another).
  • engineered patterns e.g., application specific custom patterns and textures, repetitive or random patterns, patterns created on complex geometries, with no metallurgical changes in material, a chemically pure resulting surface, and a pattern that is integral with the parent material (e.g., not a coating).
  • Application of these features achieves exemplary benefits such as: precise control of micropore size, accurate maintenance of a percentage of original surface; reduction of micromotion, and/or retention of bone chips shaved from undercut edges in texture pockets.
  • FIG. 1 it will be seen that there first is provided an article 10 of one of the above-mentioned materials, or a material similar thereto.
  • the article 10 is provided with a datum surface 12 in which it is desired to provide a multiplicity of undercut recesses.
  • a layer 14 of maskant material is deposited on substantially the entirety of the surface 12.
  • the maskant is a suitable acrylic, epoxy, or polyester resist, or the like.
  • the layer 14 may be applied by dipping, spray coating, or electrostatic depositing, or any other coating method to produce a layer thickness of about 0.001-0.010 inch.
  • the coated article of FIG. 2 preferably is baked at 200°F ( ⁇ 10°F) for about 15-17 minutes, or any sufficient combination of time, pressure (such as vacuum-baking) and temperature to insure the removal of water, as is customarily used in the art.
  • Kodak Thin Film Resist® has been found to be a quite suitable maskant. To the Kodak Resist is added 2%, by weight, carbon black pigment, or other pigment described hereinbelow.
  • the adhesion of the resist or masking agent to a metal surface of the object to be textured preferably includes of an actual chemical, ionic, or molecular bond to the metal itself.
  • the undercutting process preferably is conducted via spray impingement of the etchant, or other agitation, such as turbulence or ultrasonic cavitation, often for periods of time that are more prolonged than is generally encountered in common photo fabrication. The duration of the undercutting process is dependant upon the substrate selected and the etchant system chosen. Preferably, etching lasts up to 10-15 minutes. It may exceed 20 minutes.
  • a layer 14 of common photopolymerized polyester resist requires cleaning and abrading of the datum surface prior to application of layer 14.
  • pre-etching and pre-baking of the metal surface is sometimes required to insure the integrity of the maskant-metal bond.
  • it is desirable to remove a minute amount of surface material preferably 0.001 inches to 0.005 inches to insure a chemically clean and pristine metal surface.
  • Additional embodiments include the use of a layer 14 of epoxy dip coatings, electrostatic coatings, electrophoresis coatings or other electro-deposited coatings, and spray coatings of resist or masking agents.
  • Dispersing an appropriate pigment or dye into a maskant layer can render the maskant laser receptive.
  • the maskant is selected based on the wavelength of the laser, or any projected light source, to be used to produce the desired pattern of maskant 14 on surface 12.
  • the resulting local heating from the absorption of laser energy selectively removes tiny areas of the resist or maskant layer 14, thereby exposing the underlying metal surface 12 of the article to the action of an etchant.
  • Ordinary conventional photographic image and development techniques may be used with these photosensitive materials and methods. They are less suitable, however, for contoured parts, as artwork negatives cannot easily be laid upon them for exposure.
  • a preferred maskant is Kodak Resist, to which is added about 2% carbon black pigment, or other pigment more particularly suited to the laser wavelength to be employed.
  • the pigment is dispersed into the maskant in a high shear mixer until fully dispersed, or until a temperature rise of 15-20°C is reached.
  • the resulting maskant is applied by dipping or by spraying, spinning, brushing or electrostatically depositing onto the surface to be treated.
  • Selected areas 16 of the layer 14 are then removed to expose portions 18 of the datum surface 12.
  • the use of computer-directed direct laser ablation to generate programmed patterns in the maskant layer allows the application of such patterns to irregularly shaped finished goods, parts, or items which have surfaces of compound curves or radii.
  • Such shapes are routinely encountered in implantable medical devices, such as dental post implants, hip joint assemblies, and maxillofacial prosthetics.
  • a computer-directed laser to directly ablate the maskant or etch resist layer in selected loci is preferred.
  • FIG. 40 illustrates a preferred two-dimensional pattern 410.
  • the pattern is transferred to the surface maskant by laser ablating black regions 412.
  • the black regions 412 are then etched with undercutting until the etched regions reach the desired complex 3-dimensional arrays of cavities.
  • the resulting patterns does not superficially resemble the starting pattern, though the resulting pattern is a derivative of the starting pattern, and/or the starting patterns basic fractal elements.
  • ablations are made by direct writing with a neodymium-doped YAG laser with a wavelength of 1.06 microns, to which carbon black is receptive.
  • a pattern is selected which optimizes the effects of undercutting. The pattern chosen is saved in Tagged Image File Format (TIFF) or as a plot (PLT) graphics file, and used to direct a laser marker.
  • TIFF Tagged Image File Format
  • PHT plot
  • an Electrox, Scriba Nd:YAG laser marker may be used, with patterns stored in digital file format. Upon laser exposure, the underlying surface portions 18 are exposed in those areas in which the maskant absorbs the laser beam. The pattern produced by laser ablation is predictable and can be accurately duplicated and repeated from implant to implant. While the aforementioned YAG laser has been found effective in the present invention, so also have CO 2 , diode pump, and green lasers. Any laser capable of ablating, or thermally vaporizing, the maskant to generate a desired pattern of exposed surface may be used in carrying out the method described herein. Other methods of removing maskant include: mechanical tools, chemical milling, photo-chemical etching and laser eradication.
  • the pattern can be generated on a Computer Aided Design (CAD) system using any compatible file type, or generated as a phototool for imaging.
  • CAD Computer Aided Design
  • the pattern can be scanned from a drawing, print, photograph, or the like, and converted into any file type compatible with the laser system employed.
  • An alternative method of manufacture is to use a photo sensitive maskant, which is applied to the device as stated above, or applied as a dry film which is laminated to the surface.
  • the maskant is then exposed, using a light source of an appropriate wavelength (typically 280-550 nanometers). Portions of the maskant are cross-linked and/or bonded to the surface during the exposing process (in the case of negative working resist).
  • the other areas of the maskant are dissolved or washed away in a developing process that utilizes a compatible developer solution, such as sodium or potassium carbonate, or stoddard solvents, thereby exposing the underlying material.
  • the exposed portions 18 of the surface 12 are etched, preferably using a spray etcher at 100°F spray temperature and 10 lbs/in spray pressure, in a Nitric and Hydrofluoric Acid solution for about 20 minutes. Sufficient "fresh" etchant is continuously impinged upon the etch surfaces 18 to encourage lateral, as well as vertical etching. It will be understood that alternative etching processes, such as immersing ultrasonics and electrolytic etching, can produce similar results. In one embodiment of the present invention, the methods of replenishing the etchant at the surface being textured is required to successful practice of the invention.
  • a spray impingement method is frequently used.
  • such a spray method allows an off-axis or directional control to achieve the resulting textured surface and causes the undercutting to be in one or more desired directions or axes of the part (e.g., device 10) rather than another.
  • the spray etching system can be arranged so as not to impinge from all angles, or not to rotate with respect to the workpiece.
  • the etching produces recesses 20 which are undercut, as shown in FIG. 4, and which are, in part, interconnected, as at 22.
  • the metal is etched in such a manner as to deliberately cause undercutting of the pattern, and to permit connection, joining, or "breakthrough" of some of the recesses so as to produce a sharply defined complex network structure, including an interconnecting pattern in which the size of most of the recesses is smaller at the surface 12 than at a plane some distance below the surface 12 of the article 10.
  • the recesses 20 may, in at least some instances, interconnect at and near the surface 12, as at 22 in FIG. 4, to provide enlarged surface recesses 20a (FIG. 5).
  • etching of the metal surface 12 is thus carried out in one step, as opposed to repetitive etching suggested in some of the prior art references cited hereinabove.
  • prefe ⁇ ed one-step etching process non-spherical ovoid shaped recesses are created featuring desired sizes and depths which are repeatable from implant to implant.
  • the remaining resist may be removed by immersing the body surface in a NJ/Phase 23 Stripper bath at about 180°F for about 10 minutes.
  • the maskant layer may be removed (FIG. 5) by solvation or emulsification.
  • the article 10 may be lightly post-etched.
  • the metal was first washed with an alkaline degreasing detergent (e.g., an Oaktite® solution), water-rinsed in de-ionized water and briefly pre-etched in a hydrofluoric/nitric acid etchant solution, so as to produce a chemically clean, freshly-exposed metal surface suited to maskant adhesion, water-rinsed again thoroughly, and oven dried at 110°C prior to coating with the selected resist agent (e.g., Kodak KPFR, or any other resist, including other polymer classes, such as reactive epoxy or urethan systems, or lacquers and varnishes).
  • an alkaline degreasing detergent e.g., an Oaktite® solution
  • a hydrofluoric/nitric acid etchant solution e.g., a hydrofluoric/nitric acid etchant solution
  • a polyester resist coating was then applied by dipping, air-drying for 15 minutes, and baking at 100°C for 20 minutes.
  • an epoxy e-coating e.g., PPG Powercron® CF-665
  • a desired pattern may then be laser-imaged onto the surface with a 90 watt neodymium- doped YAG laser at 85% power, and at a machine setting of 3 frequency units to achieve a shallow penetration to and below the surface of the base metal. The typical depth of penetration is 10 microns. This assures the cleaning of the metal base layer to remove maskant ablation residues from the regions to be etched.
  • the hip joint was then again baked at 100°C prior to etching to insure full cross-linking of the polymer, and to remove low- molecular-weight pyrolysis products from the maskant polymer.
  • the surface of the hip joint was then etched to the desired depth.
  • the broadest depth range is 0.1mm to 2mm, with a prefe ⁇ ed depth range of 0.4 to 0.6 mm.
  • Certain patterns may, in extreme situations on some metals require shallower or deeper etching than the prefe ⁇ ed range, in order to develop a desired three-dimensional pattern. For example, more delicate pattern designs, may require very light etching in order to preserve the original pattern details.
  • nearly all the patterns used to date have been well-formed by etch depths of 0.4 to 0.6 mm.
  • the depth range preferably depends on pattern coarseness. In one embodiment, coarser patterns have wider land areas (discussed below), and therefore can tolerate deeper etch depths before they are cut off by undercutting in a vertical spray etcher at 20 to 30 minutes (depending on desired depth and pattern coarseness) at 100°F.
  • the article After etching to the desired depth the article is rinsed well in running water and air dried. The article is then inspected for proper etching, sufficient undercutting, and general quality. The resist or maskant was then stripped from the hip joint using a nuphase stripper solution such as a concentrated caustic stripping solution (e.g., Oakite® Eurostrip® 704 manufactured by PC&E), at a temperature of 160°F, for 15 minutes. After stripping, the article was rinsed in deionized water and oven dried at 220°F.
  • a nuphase stripper solution such as a concentrated caustic stripping solution (e.g., Oakite® Eurostrip® 704 manufactured by PC&E), at a temperature of 160°F, for 15 minutes.
  • a method for producing a complex, at least in part interconnecting pattern, or similar 3-dimensional surface treatment, to enhance the attachment of biological matter to a surface of an implantable device, or the interconnection of other bodies to be bonded made by selective etching and undercutting of a surface so as to form a network of at least in part interconnected recesses.
  • the pattern is formed by the direct laser ablation of an etch resist or maskant layer, allowing the textured surface to be applied to items with complex or curved surface geometries.
  • the pattern is stored in a CAD or other computer-based system which controls the maskant ablations and is predictable and subject to repetitive duplication.
  • the article is chemically etched to form the complex pattern.
  • the metallurgical properties of the material of the article are not altered by heat, but remain substantially consistent during the process.
  • Soft tissue or bone may in-grow the surface so produced, resulting in an interpenetrating network that offers superior mechanical adhesion and resistance to degradation.
  • the sharp edges at the intersections of the undercut recesses and the original datum surface facilitate an initial "scratch- fit" between the implant surface and a bone.
  • a selected pattern of undercut and at least in part interconnected recesses is effected in a surface of the surgical implant (FIG. 5).
  • the implant surface 12 is pressed against the bone B, (FIG.
  • the scratch-fit securely adjoins the implant article 10 to the bone B, to prevent or minimize micro motion between the body 10 and bone B.
  • the presence of such motion would discourage the ingrowth of bone into the implant and thereby discourage the long-term interconnection of the implant and bone.
  • the scratch-fit application of the implant to the bone harvests bone particulate matter which falls into the surface recesses and is retained by the recesses to encourage and stimulate ingrowth of the bone into the recesses.
  • the recesses are of an ovoid configuration, they provide a greater sub-surface fractal area than spherically shaped recesses, and thereby a greater area for engagement of the bone material and the implant.
  • the milling of the host bone B may further serve to ream the bone B to the precise size and configuration of the article 10, insuring the best possible fit.
  • appropriately shaped and sized buns of the texture on article 10 are preferably furnished to pre- form a receptacle in the bone to properly receive the article 10.
  • the scratch-fit securely adjoins the implant article 10 to the bone B, to prevent or minimize micro motion between the implant 10 and bone B. The presence of such motion would discourage the ingrowth of bone into the implant and thereby discourage the long-term interconnection of the implant 10 and bone B.
  • a device with a textured surface according to the present invention can affect a self-fitting function.
  • a textured surface according to the present invention, is applied to an acetabular cup, the cup itself can be used as a reaming tool, effecting a perfect fit to the host bone and shortening healing time.
  • the resulting material is forced into the recesses to serve as a nucleation host for a spontaneous homograft completed by the attraction and growth of the patient's osteoblasts, providing a strong bond and longer installed lifetime.
  • Some embodiments of the present invention may incorporate sharp-edged geometry such as at undercut 3 (See FIG. 12). It may be desirable for the sharp-edged undercut geometry to be later modified by a subsequent dulling process so as to causes sharp edges to be rounded. For example, abrasive blasting, glass bead blasting, or a subsequent acid etch all may be used to slightly dull or "break" the original sharp edges, if desired. Such a subsequent dulling process may include, for example, etching, polishing (e.g., electropolishing), abrasive reduction, buffing, and honing. Through this process, at least some of the walls 7 (shown on Fig.
  • FIG. 14 illustrates a prefe ⁇ ed geometry of a cavity 20 which has been deliberately produced with the geometry of a complex ellipsoid.
  • a complex ellipsoid is preferably derived from two or more ellipsoids.
  • the complex ellipsoid is derived from at least two non-spherical ellipsoids.
  • Alternative embodiments may include combinations of spherical and non-spherical ellipsoids.
  • the complex ellipsoids may be a combination of ellipsoid 30a and ellipsoid 30b.
  • the complex ellipsoids may alternatively combine three or more ellipsoids with three or more different angular projections.
  • a geometric shape of the illustrated cavity 20 may be described as being defined, at least in part, by two non-spherical ellipsoids sharing a major axis 9 and having varying angular projections (e.g., an ellipse having a 40 degree protection, superimposed on an ellipse having a 50 degree projection, or any combination of ellipses from about 9 degrees to about 89 degrees so as to produce a species of the complex ellipse shape).
  • Ellipsoid 30b with a narrower angular projection defines a bottom 4 of cavity 20.
  • Ellipsoid 30a with a wider angular projection defines an arched undercut 3 which is contiguous with wall 7 and bottom 4.
  • wall 7 and bottom 4 are concave and contiguous.
  • Cavity 20 (FIG. 16) may be further characterized as having a ratio of cavity width, w, to cavity depth, d, that is greater than or equal to unity.
  • the preferable width:depth ratio ranges from 1:1 to 9:1. In a prefe ⁇ ed embodiment, the ratio is approximately 4:1.
  • protrusions 2a, 2b, and 2c have differing geometries each of which is preferably defined by the relationship between at least two complex ellipsoids.
  • Protrusions 2a, 2b, and 2c extend from bottom surface 4 of cavity 20 toward datum 12.
  • Protrusion 2a has a peak 5a in the form of a plateau or mesa which is coincident with outer surface 12.
  • Complex ellipsoids 1 la and 1 lb define the lateral dimensions of protrusion 2a.
  • Cavity 20 is also defined by complex ellipsoids 11a and l ib which intersect datum 12 to create cavity 20 in outer surface 12.
  • protrusion 2a The portion of outer surface 12 remaining untouched by the ellipsoids 1 la, 1 lb defines peak 5a.
  • An ellipsoid forming protrusion 2a preferably forms an undercut 3 at the face of the protrusion.
  • Protrusion 2c has a sub-peak 5c located between datum 12 and bottom 4. Sub-peak
  • protrusion 5c is defined by the intersection point of at least two complex ellipsoids 11.
  • protrusion 2c is formed from the at least two complex ellipsoids 1 la, 1 lb, which overlap to the extent that no overhang is created in wall 7 of protrusion 2c.
  • the overlapping of ellipsoids may result in an overhang on one face of the protrusion but not on another face of the same protrusions.
  • Protrusion 2b has an intermediate peak 5b which is also located between datum 12a and bottom 4.
  • Intermediate-peak 5b is preferably defined by two or more complex ellipsoids 11a and 1 lb that do not overlap.
  • the complex ellipsoids 11a, l ib that at least partially define intermediate-peak 5c, however, are in close enough proximity to each other that the portion 140 of article 10 that previously existed between intermediate-peak 5c and datum 12a can be predicted to break-off during manufacture such as, for example, during polishing of the etched product, leaving an intermediate peak 5c.
  • the surface is "softened” by common buffing or polishing methods (as described above). Thus, in one embodiment, the surface is modified such that the sharp edges will be removed, as well as some of the tops of the proj ections .
  • FIGS. 14 and 16 shows the major axis 9 substantially parallel with datum surface 12.
  • Orientation of the major axis may vary from perpendicular to parallel depending on the desired finished texture, the pattern of the desired texture and direction of the texture.
  • Prefe ⁇ ed embodiments have an orientation of axis 9 that varies between 90 degrees and 70 degrees relative to datum 12.
  • axis 9 is oblique to datum surface 12 (shown in Fig. 16A). This is preferably achieved by impinging etchant at an acute angle to datum surface 12.
  • an asymmetrical undercut pattern that is characterized by an undercut face 165, of ellipsoid 166, that projects over cavity 20 a distance greater than the projection of the opposing face 164.
  • opposing face 164 does not overhang cavity 12.
  • the impingement of etchant at an angle produces a tilted saw-tooth or tiger-tooth structure 169 shown in FIG. 16B.
  • Such structure allows relatively easy insertion into a bone channel 168 (e.g., when insertion is in a direction such that undercut 165 is not urged into bone B as in FIG.
  • cavities 20 are aligned in series so that a cross-section of the textured surface has a regular pattern which may also be a repeating pattern (see, e.g., FIGs. 16C, 16D), 42A and 42B).
  • FIGs. 42 A and 42B illustrate a comparison between the affects of directional and nondirectional impingement.
  • FIG. 42B illustrates an embodiment of the invention where nondirectional impingement has been performed.
  • the major axis 9 of complex ellipsoid 30 is substantially parallel with datum surface 12, and undercuts are present at the point 432 where the cross section of ellipsoid 30 intersects datum 12.
  • major axis 9 is oriented oblique to datum surface 12, there is an undercut 432 at the distal end 431 of cavity 20, and face 434 has no undercut at the proximate end 433 of cavity 20.
  • cavity 20, formed by directional etching is defined by a concave surface 432 and a convex surface 434.
  • opposing surfaces of cavity 20 may each have concave configurations (FIGs. 16C and 16D).
  • unidirectional barbs 422 are produced in the surface that can be inserted into bone or tissue.
  • the directional orientation of barbs 422 make it difficult to withdraw from the bone or tissue.
  • simpler non-directional agitation such as a turbulently- flowing etchant bath, or ultrasonic cavitation can be employed.
  • FIG. 16 illustrates a prefe ⁇ ed geometric relationship between surface 12 and ellipsoids 30a and 30b.
  • the dimensions are typical and descriptive of a commonly achieved pattern, but are not restrictive. The skilled practitioner may vary these dimensions greatly depending on the desired outcome.
  • depth d of cavity 20 as measured from the datum 12a to bottom 4 is substantially 0.0210 inches.
  • Major diameter a of ellipsoids 30a and 30b is substantially 0.0474.
  • the distance b from datum 12 to the major axis 9 is substantially 0.0055 inches.
  • Distance c along the major axis 9 between the perimeter of complex ellipsoid 30a to a point x projecting from the intersection of complex ellipsoid 30a with datum 12a is substantially 0.0012 inches. It follows, that distance e along major axis 9 between projection points x and y is substantially 0.0450 inches.
  • Texture 130 is embodied in an article 10 after the etching process described above.
  • three dimensional pattern 130 may be of an i ⁇ egular pattern to the extent that the structural features of the pattern are unevenly distributed on a micro-level, this pattern is both repeatable across the device, and reproducible between devices.
  • pattern 400 may be seen by an observer.
  • the patterns are written into or through the maskant or etch resist layer by a laser as described herein.
  • the pattern is displayed as an image that can be seen by an observer on a computer monitor, printed output, or other such viewing device.
  • pattern 400 may be derived from an initial pattern having a regular series of elements that include one or more regular or i ⁇ egular geometric configurations such as circular dots, squares, prisms, parallelepipeds, trapezoids, triangles, hexagons, and other such geometric shapes that the practitioner deems suitable to generate the third-dimension development of the desired finished texture 130.
  • a pattern of repeated fractals or other pseudorandom network of elements are employed to generate the initial pattern.
  • patterns In practice when patterns are developed into three-dimensional patterns 130 by etching, they generally regularize rather than randomize. For example, an a ⁇ ay of dots or other shapes will form boundaries as the su ⁇ ounding material is removed by etching.
  • a connection density of portions of the etched surface peaks, sub-peaks, and intermediate peaks of approximately 58% is reached, a phenomenon known as "percolation threshold" forms, where networks of connections form.
  • FIGs. 17A, 17B, 17C, 17D, and 17E illustrate variations on the textured surface of the prefe ⁇ ed embodiment.
  • FIG. 17A illustrates textured surface 170 having a three-dimensional i ⁇ egular pattern that is characterized by multiple intersections of complex non-spherical ellipsoids that form peaks 5a and 5c.
  • sub-peak 161 which is defined by a the intersection of at least two complex ellipsoids.
  • a first complex ellipsoid defining sub- peak 161 further defines, at least a portion of cavity 162.
  • This configuration further illustrates a resulting texture where intersecting complex ellipsoids of varying angular projections are oriented with major axes at an offset angle to one another.
  • the initial pattern used includes elongated elements, or sets of two or more dots, a first set oriented at one angle to a grid, and a second set oriented at another angle
  • the etching and undercutting process will generate a series of ovoid shapes as viewed from the top, with long axes aligned to these grid lines.
  • one set of grid lines may be at an angle of 40 degrees to the other, resulting in a lozenge-shaped array.
  • FIG. 17A Also illustrated in FIG. 17A is the effect of a scratch-fit where soft tissue shavings 160 have migrated into the voids 20 and are growing to fill the voids.
  • FIG. 17B illustrates textured surface 171 having a regular pattern.
  • Each protrusion 2a in FIG. 17B has peak 5a coincident with outer surface 12 (not illustrated).
  • a geometry characterizing protrusion 2a that is defined by four (4) complex ellipsoids which have been uniformly oriented.
  • Further characterizing this embodiment is a distance, f, between protrusions that is uniform among transverse and longitudinally adjoining protrusions.
  • distance f between protrusion 165a and 165b is substantially the same as the distance, g, between 165b and 165c.
  • the distance between transversely adjacent protrusions may be different from the distance between longitudinally adjacent protrusions thus forming a "rectangular pattern" as opposed to a "square pattern”.
  • Any other geometrically uniform patterns are also within the scope of this invention. These include, as examples, ellipsoidal cavities substantially a ⁇ anged on a hexagonal, pentagonal, triangular, or other regular geometric lattice. FIG.
  • 17C illustrates a uniform repeating pattern that combines a plurality of protmsion geometries including protrusions 166a defined by five (5) complex ellipsoids; protmsions 166b defined by four complex ellipsoids; and sub-peaks 166c defined by three complex ellipsoids 166c.
  • the horizontal orientation of adjoining protmsions varies in a substantially non-random pattern.
  • FIG. 17D illustrates protmsion 167b that is defined by a multiplicity of complex ellipsoids.
  • Protmsion 167b has peak 167a that has been formed to project a scalloped surface 177.
  • intermediate peak 175 and sub-peak 176 There is also shown intermediate peak 175 and sub-peak 176.
  • intermediate peak 175 has one face that is not undercut, or with undercut regions have been etched away in the process, and another face that is undercut.
  • FIG. 17E illustrates protmsion 168 that has been defined by a multiplicity of complex ellipsoids.
  • protmsion 168 extends for a predetermined length of the surface.
  • the predetermined length forms a rib.
  • the top of rib 168 is preferably coincident with the datum surface 12.
  • rib 168 has a sub peak or an intermediate peak.
  • rib 168 has a combination of peaks, sub-peaks, and intermediate peaks.
  • each face 17 of protmsion 168 has an undercut surface.
  • protmsion 169 which is characterized by an intermediate peak 5b that was formed when the base material above the peak was broken-off, or where a top section became isolated or cut away by the interception of undercut regions. While some textured surface applications benefit from an undercut textured embodiments, the methods of the present invention can be used to create engineered articles. For example, certain embodiments are suited for creating an implant article having a mesh- and plate-surface (described below). In other embodiments, undercut textured surfaces are combined with mesh-and-plate surfaces. To make a mesh-and-plate surgical implant, there is provided a thin sheet 180 (FIG. 18) of tissue and bone compatible metal, such as titanium. A maskant layer 192 (FIG.
  • the maskant layers 192, 196 cover substantially the entirety of the first and second faces 194, 198, respectively.
  • the maskant layers 192, 196 are resistant to chemical attack. It has been found that a photo-chemical resist, such as duPont Riston®, or Kodak Thin Film Resist®, serve as appropriate materials for the maskant layers 192, 196.
  • the maskant layers 192, 196 are then in part ablated from selected portions of the metal faces 194, 198 (FIG. 20), as by mechanical tools, chemical milling, photo-chemical etching, or by laser eradication, to expose portions 202, 204, 206 of the respective metal faces 194, 198 in desired patterns, ready for etching.
  • the exposed portions 204 of the first face 194 and the maskant layer 192 on the first face 194 are covered with a protective tape 210, leaving exposed only the region 202 where a central through-hole is desired for acceptance of a mounting screw (not shown).
  • the exposed portions 206 of the second face 198 and the maskant layer 196 on the second face 198 are covered with a protective tape 212.
  • the tapes 210, 212 may be 3M Brand Type #1280 Platers Tape.
  • the through-hole region 202 is then subjected to etching, for example, as by spray or immersion, using an acid bath of a mixture of nitric and hydro fluoride acid. It is prefe ⁇ ed, during the etching process, to periodically remove sheet 180 from the etching process and rinse, dry and bake the sheet to maintain the integrity of the maskant and allow for in-process inspections.
  • the protective tape 210 is removed (FIG. 23) and the etching of the crater 222 is resumed, and etching of the exposed portions 204, constituting the mesh portion of the implant, is undertaken.
  • the exposed metal regions 222 and 204 are progressively removed by the etchant (FIG. 24). The etching continues until the removal of metal from the first face 194 and crater 222 has reached the predetermined extent desired (FIG. 25).
  • the second tape 212 is then removed, exposing the maskant layer 196 and exposed portions 206 on the second face 198, including an area 252 opposite the crater 222.
  • Etching of the through-hole area 252 in the sheet face 198 breaks through to the crater 222 to effect a counter-sunk through-hole 262 (FIG. 26) and second face openings 264 in communication with the newly etched first face 266.
  • the first and second maskant layers 192, 196 are then removed (FIG. 27), leaving an implant device having the mesh portion 272, a plate portion 274, and at least one through- hole 262 for receiving a mounting screw.
  • FIG. 28 there is shown, for illustrative purposes, a dog-leg plate portion 274 having one or more through-holes 272 therein, the plate portion 274 being bounded by the mesh portion 272.
  • FIG. 29 there is shown a divided plate 292 having through-holes 262 therein, and bounded by the mesh portion 272.
  • through-holes 262 may be provided in mesh portions 262, such through-holes preferably being su ⁇ ounded by rim collars 302 comparable in thickness to a plate portion 274.
  • the through-holes 262 preferably are countersunk to receive mounting screws.
  • the maskant layers 192, 196 may be exposed to a movable laser beam which is moved in accordance with a path governed by a CAD data file, wherein the beam removes unwanted maskant. After the laser removes the maskant, the sheet 180 is exposed to heat and/or ultraviolet light to cure and harden the remaining maskant.
  • the mesh portions 272 preferably are of a thickness of about .5 mm and are readily flexed to follow the curvature of a bone.
  • an improved method for making an article such as a mesh-and- plate surgical implant including both bendable perforated mesh portions and relatively rigid plate portions, wherein the bendable or comfortable perforated portions are integral with and kinematically related to the rigid plate portions.
  • the improved method further provides through-holes for receiving mounting screws during implantation.
  • tissue implants may be enhanced by textured surface having undercut characteristics and/or mesh-and-plate characteristics.
  • a textured surface is specified to promote osseointegration an undercut texture may be specified.
  • a mechanical securement e.g., a screw or bolt
  • the mesh-and-plate texture may be specified. It should be recognized that combining one or more of such textures on a single implant is a viable alternative within the scope of this invention.
  • FIG. 31 illustrates tissue implant 310, constmcted from a bio-compatible material such as metal, glass, plastic, and ceramic.
  • the bio-compatible material is chemically pure (CP) titanium.
  • Implant 310 is useful in any application in which a secure attachment to an object is desired and would be enhanced by using a textured surface such as discussed herein. Though dental applications and spinal applications have different mechanical objectives, the present invention is useful in both applications.
  • Spinal devices for example, preferably separate vertebrae in permanent alignment and transfer compressive forces between adjacent vertebrae. Bone ingrowth secures these devices into place, especially with the object of resisting forces that would tend to dislodge them.
  • Dental devices for example, are preferably screwed into a hole bored in the mandible, whereupon bone ingrowth locks them into place so that teeth or other appliances can be affixed to them.
  • dental devices must resist tensile and compressive forces and transfer those forces to the bone sufficiently that the bone-to-appliance bond strength is not exceeded.
  • implant 310 is useful for implantation and/or attachment to hard tissue such as bone in spinal and dental applications and soft tissue.
  • implant 310 may be adapted for use in a commercial spinal fusion device.
  • Another embodiment of implant 310 may be adapted for use in dental applications, such as with a dental implant in tissue.
  • implant 310 is particularly well suited as a dental implant post onto which prosthetic teeth or other appliances may be attached.
  • Implant 310 has a longitudinal axis 311. Distal end 312 of implant 310 typically is inserted into tissue such as a bone (e.g., a jaw bone). In one embodiment, proximal end 314 may be adapted to receive a prosthesis such as an artificial tooth or other dental appliance.
  • implant 310 preferably has a wall 320 that is disposed about longitudinal axis 311.
  • wall 320 is radially disposed about axis 311, and wall 320 has an outer face 322, and an inner face 321.
  • one or both of outer face 322 and inner face 321 may be substantially parallel to axis 311.
  • wall 320 is tapered such that distal end 312 of wall 320 has a smaller diameter about axis 311 than at proximal end 314 of wall 320.
  • wall 320 defines cavity 324.
  • wall 320 includes one or more apertures 318 which permit the transmission of fluids (e.g., blood), tissue, and tissue fragments (e.g., bone fragments) into cavity 324 to promote, for example, tissue inter-growth (i.e., osseointegration) and/or a heat and/or tissue venting.
  • Aperture 318 may be formed by any method including the methods described herein or other mechanical methods (e.g., drilling), chemical methods(e.g., chemical etching), and/or heat methods(e.g., laser).
  • apertures 318 are formed by chemical etching of one or both of outer surface 322.
  • aperture 318 may be more specifically formed by a chemical etching process applied to outer surface 322.
  • aperture 318 is formed by laser ablation and chemical etching process applied to both outer surface 322 and inner surface 321 such as the method used to create countersinks, mesh geometries and textures as described in U.S. Patent application Nos. 09/976,722 to Amrich et al., and 10/021,616 to Amrich; the entirety of each being incorporated herein by reference.
  • aperture surface 323 there is at least one aperture 318 that is defined by aperture surface 323, extending between inner face 321 and outer surface 322.
  • Aperture surface 323 may be of any geometry.
  • aperture surface 323 is substantially flat (e.g., is substantially in a two dimensional plane).
  • aperture surface 323 is curved such as concave, convex or a compound curve (e.g., a curve with both a concave and a convex component, and multiple concave or convex curves of varying radii and combinations thereof).
  • aperture surface 323 is disposed normal to axis 311.
  • aperture surface 323 is oblique to axis 311. Where aperture surface 323 is oblique to axis 311, that angle may be either acute or obtuse. Aperture surface 323 may also be disposed at varying angles to inner face 321 and outer surface 322. In a prefened embodiment, aperture surface 323 is at least partially a textured surface 351 as illustrated in FIG. 35 and as disclosed herein. In one embodiment, the textured surface 351 of aperture surface 323 has a texture that is characterized by undercut recesses such as is created from the methods described herein. Aperture 318 may be of varying sizes depending on their intended function. Aperture
  • aperture 318 can have any shape including curved (e.g., round aperture 371), angular (e.g., square aperture 372 and triangular (not shown)), complex geometric shapes (e.g., multi-curved aperture 373) and combinations thereof within any one aperture 318 or among different apertures 318 of the same implant 310 (as illustrated in FIG. 37A).
  • aperture 318 has an oblong geometry with the maj or axis of aperture 318 longitudinally oriented and the minor axis transversely oriented to axis 311 as illustrated in FIG. 37C.
  • Implant 310 may have one or more aperture 318.
  • apertures 318 are either angularly disposed to one another (e.g., less than 180° apart along face 321), longitudinally disposed (e.g., aligned along the longitudinal axis), disposed across from one another (e.g., at 180° relative to face 321), and in geometric combinations thereof. Apertures 318 may extend into the self-tapping region (discussed below) of implant 310.
  • one or both of outer wall 322 and inner wall 321 include one or more recesses 362 that do not extend through wall 320.
  • Recesses 362 may be formed by any method as described with respect to aperture 318 and may include any attribute of size, shape, and/or configuration discussed with respect to aperture 318. Furthermore, any portion or all of recess 362 may include a texture surface as described.
  • implant 310 may also include one or more protmsions 325 from outer face 322.
  • protmsions 325 may be one or more ribs 326.
  • ribs 326 may be helically disposed about longitudinal axis 311 to form threads 316 as illustrated in FIG. 31.
  • An implant 310, having threads 316 may typically be installed by screwing implant 310 into tissue (e.g., bone).
  • thread 316 is continuous from a point approximately at distal end 312 to a point approximately at proximal end 314.
  • threads 316 may be discontinuous. Where thread 316 is discontinuous, the discontinuity may be at a location proximate to aperture 318 as illustrated in FIG. 31 , or the discontinuity may be located where there is no aperture as illustrated in
  • protmsions 325 are in the form of longitudinal ribs 382 (as illustrated in FIG. 38A and 33) longitudinally disposed on implant 310 such that ribs 382 n generally between proximal end 314 and distal end 312. In one embodiment ribs 382 mn generally parallel to axis 311. In another embodiment, angular ribs 383 may be disposed at an angle relative to axis 311, as illustrated in FIG. 38B. In another embodiment, transverse ribs 384 are disposed to form substantially concentric rings that are radially disposed about axis 311 as illustrated in FIG. 38D. Transverse ribs 384 can have any desired pitch angle. In one embodiment, transverse ribs 384 have a low pitch angle.
  • transverse ribs 384 have a pitch angle of substantially 0°. While longitudinal ribs 382, angular ribs 383, and transverse ribs 384 are shown to be substantially continuous from distal end 312 to proximal end 314, such ribs having discontinuities are also within the scope of the present invention.
  • ribs 326 may be in the form of discrete segments 335 protmding from wall 320. In one embodiment, discrete segments 335 are evenly distributed about axis 311. In one embodiment evenly spaced discrete segments 335 are of substantially uniform size. In another embodiment, discrete segments 335 are of varying sizes. In another embodiment, discrete segments are unevenly spaced.
  • Ribs 326 may have any cross sectional geometry including v-shaped, keystone shaped (e.g., rib 343), curved (e.g., rib 344), trapezoidal with an exterior short face (e.g., rib 348), trapezoidal with an exterior long face (e.g., rib 347), undercut (e.g., rib 345), hourglass (e.g., rib 349) and square (e.g., rib 346), as shown in FIG. 34.
  • ribs 326 on implant 310 are in the form of longitudinal ribs T32 having one or more of several geometries as shown in Figs 32, 33, 34.
  • pilot hole it may be necessary, in some procedures, to drill at least one pilot hole or successively larger pilot holes to accommodate implant 310 prior to screwing implant 310 into the tissue.
  • those embodiments having non-helical ribs are suited for tapping in place while those embodiments including threaded ribs are suited for screwing in place.
  • implant 310 may be configured to include a self-tapping thread 317 that is helically disposed about longitudinal axis 311 , as shown in FIG. 31.
  • self-tapping threads 317 are employed, installation may be accomplished with no pilot hole or with smaller diameter pilot holes than if the self-tapping thread 317 was not included.
  • Self- tapping threads 317 of a prefe ⁇ ed embodiment has a thinner web thickness and more root dimension than crest spacing. The ribs may therefore, appear to be more widely spaced apart.
  • sufficient anchoring can be achieved while reducing the amount of material (e.g., tissue) that is cut or displaced.
  • the tapping force requirement to install a device with the self-tapping features is lower than is necessary for non self-tapping threads.
  • threads T13 on implant 310 include one or more portions that are non self-tapping threads. For example, in one embodiment, only a distal portion of the threaded area of implant 310 is self-tapping. As shown in a prefe ⁇ ed embodiment of FIG. 32, protmsions according to the present invention, have a height, h, suitable to restrict removal of implant 310, for example, by the application of axial, longitudinal, and/or radial force.
  • outer face 322 and ribs 326 are textured over substantially their entire surface.
  • outer surface 322 and ribs 326 have textured portions and portions that are relatively smooth (e.g., not textured). More particularly, where a portion of ribs 326 are relatively smooth, that portion may be the crests 392 of ribs 326 as shown in FIG. 39A.
  • outer face 322 is at least partially textured, and ribs 326 are non-textured. Leaving crests 392 without texture is believed to facilitate the installation of implant 310, for example, by avoiding excessive fragmentation to tissue (e.g., bone) su ⁇ ounding the distal end of implant 310.
  • outer surface 322 is textured and ribs 326 are not textured. In other embodiments regions of texturing and non-texturing may be used on inner face 321, outer surface 322, aperture surface 323, and ribs 326.
  • inner face 321 is textured as illustrated in FIG. 39B. In another embodiment, inner face 321 is textured and there are alternating regions of outer surface 322 that are textured as illustrated in FIG. 39C.
  • an anti-rotation fixture (which may include a hollow cross-drilled stmcture) that locks the screw device into permanent immobility when bone ingrows the fixtures Such a stmcture may further serve as a vent during installation.
  • the locking mechanism is integral to the surface of a portion of the threads thus eliminating the need for an additional anti-rotation fixture.
  • an anti-rotation fixture characterizes approximately one-third of the device.
  • a textured surface may be described as having a higher fractal dimension than a non- textured surface.
  • the fractal dimension may be specified based upon the nature of the implant. For example, where the scratch- fit properties of the implant (e.g., as described above) is of primary importance, a greater fractal dimension may be specified to improve the tissue harvest during implantation. Alternatively, where strength of the bond created by the thread alone is of primary importance, a lower fractal dimension may be specified to limit the dismption of host tissue during implantation.
  • single implant may have regions of varying fractal dimensions that may be dictated by the function of each region on the implant.
  • a distal region of the implant that anchors the implant in a tissue, has a lower fractal dimension than a more proximal region that is designed with a preference toward the promotion of tissue growth over short term strength.
  • regions of higher and lower fractal dimension may alternate along the longitudinal axis 311.
  • a textured component on implant 310 is designed to promote a scratch-fit with tissue that accepts implant 310
  • the scratch- fit is believed to promote faster healing time by, for example, auto-grafting the patient's bone into the interstices of the surface geometry and causing less compressive trauma to the bone.
  • the interference fit of the appliance 310 into the prepared site causes the patient's bone B to be shaved by the sharp edges of the surface texture. Since the bone matter is "donated" by the patient, the resulting autograft allows faster healing than is possible with bone matter provided by bone bank donors.
  • the bone matter in one embodiment, originates from the patient and does not need to be denatured, or otherwise have its vitality compromised.
  • the bone matter is instantly used as a growth lattice with no local immune reactions.
  • the bone matter may thus be regarded as "alive". Even where a textured surface does not scratch the tissue, it provides a bedding upon which tissue fragments may accumulate and seed.
  • the elliptical cavities of the textured surface becomes filled with the shavings from the patient's bone without compromising the vitality of shavings and thus not requiring a denaturing step. This bone matter is, therefore, instantly available for growth lattice without local immune reactions.
  • the higher fractal dimension of the textured surface (relative to a non-textured surface) is believed to ensure a higher shear strength of the bond between the implant and the host tissue.
  • ribs 393 are believed to initially retain the implant.
  • implant 310 is tapered about axis 311
  • the taper promotes harvesting of bone into the textured surface.
  • the widening shape generates radial forces that act as a progressively tightening fit.
  • Pin pushout strength refers to a test where candidate textures are applied to small metal dowels. Holes are bored into femur bone in a test subject (canine), and the test sample dowels are pressed into the bores, using a fixture to assure straight and uniform placement. After sufficient time is allowed for healing and bone growth, the bone is removed by pressing the dowel with a pin. The amount of force required to press out the dowel with the pin is measured and recorded by an Instron® tester or similar apparatus. This measures the shear strength of the bone-to-implant bond.
  • Tests were performed to compare some embodiments of the present textured surfaces with those of known textured surfaces.
  • the tests include quantifying the degree of roughness attributable to these competing embodiments and comparing that roughness to the effectiveness of an implant bonded with the embodied textured surfaces.
  • the degree of roughness was quantified using the fractal analysis program BENOIT v.1.3, (developed by Trusoft International, Inc. of St. Russia).
  • the simplest method of measuring the fractal dimension of a surface is to photograph a cross section of the prepared surface, and render the outline as a simple white line on a black background in an image stored as a bitmap (BMP) file for processing by the program. If such a line is superimposed on a grid, and the number of boxes penetrated by the line is counted, and repeated at successively smaller box sizes, then plotted in log-log axes, a scale- independent number is reached.
  • BMP bitmap
  • the box dimension is defined as the exponent Db in the relationship:
  • N(d) is the number of boxes of linear size, d, necessary to cover a data set of points distributed in a two-dimensional plane.
  • the basis of this method is that, for objects that are Euclidean, Eq. (la) defines their dimension.
  • This dimension is sometime called grid dimension because for mathematical convenience the boxes are usually part of a grid.
  • the overestimation of N(d) in a grid dimension is not a function of scale (i.e., we overestimate N(d) by, say, 5% at all box sizes d), which is a plausible conjecture if the set is self-similar, then using boxes in a grid or minimizing N(d) by letting the boxes take any position is bound to give the same result. This is because a power law such as Eq. (la) is such that the exponent does not vary if we multiply N(d) or d by any constant.
  • a choice to be made in this procedure is the range of values of d. Trivial results are expected for very small and very large values of d. A conservative choice may be to use as the smallest d ten times the smallest distance between points in the set, and as the largest d the maximum distance between points in the set divided by ten. Alternatively, one may exceed these limits and discard the extremes of the log-log plot where the slope tends to zero.
  • the grid should be overlaid in such a way that the minimum number of boxes is occupied. This is accomplished in Benoit by rotating the grid for each box size through 90 degrees and plotting the minimum value of N(d). Benoit permits the user to select the angular increments of rotation.
  • the Information Dimension is often encountered in physics literature, and is generally different from the box dimension.
  • box dimension a box is counted as occupied and enters the calculation of N(d) regardless of whether it contains one point or a relatively large number of points.
  • the information dimension effectively assign weights to the boxes in such a way that boxes containing a greater number of points count more than boxes with less points.
  • the information entropy 1(d) for a set of N(d) boxes of linear size d is defined as
  • M is the number of points in the i-th box and m is the total number of points in the set.
  • the following table illustrates the relationship between the Information Dimension of certain textural products and the Pin Pushout strength for selected products. Also illustrated in the following table is the standard deviation of the Information Dimension as calculated by the Benoit software. Higher standard deviations number are illustrative of a more "random", less ordered surface texture.
  • textured portion 351 has any desired texture depending on the particular use of implant 310.
  • textured portions 351 may include patterns formed from the methods described herein. Textured portions may also include random patterns as described in U.S. Patent No. 5,258,098, U.S. Patent No. 5,507,815, U.S. Patent No. 5,922,029, and U.S. Patent No. 6,193, 762 each issued to Wagner et al., the entire contents of which are hereby incorporated by reference.
  • the textures may also include the patterns described in U.S. Patent No. 5,975,903 issued to Shoher et al., U.S. Patent No.
  • a typical hip-replacement assembly or prosthesis, includes a femoral stem 4302 having a neck portion 4304 to which there is fixed a ball-like head 4306.
  • the head is received in a lining 4308, which is disposed in an acetabular cup 4510.
  • the acetabular cup 4510 is provided with a datum surface 12, which is adapted for engagement with a bone.
  • the datum surface 12 is provided with a multiplicity of undercut micro recesses 20, described hereinbelow.
  • the micro recesses 20 may be provided in accordance with methods set forth above.
  • a complex, at least in part interconnecting pattem, or similar 3-dimensional surface which enhances the attachment of bone to the surface of the implant.
  • undercut micro recesses 20 are produced as follows:
  • the acetabular cup 4510 of one of titanium, zirconium, stainless steel and alloys thereof, tantalum, refractory metals, metal carbides, cobalt-chromium, and alloys thereof, and ceramics, plastics and glass, and composites of metals, ceramics, plastics, and glass, or a material similar thereto.
  • the cup 4510 is provided with the datum surface 12 (FIG. 45) in which it is desired to provide a multiplicity of undercut recesses 20.
  • a layer 14 of maskant material is deposited on substantially the entirety of the datum surface 12.
  • the maskant is a suitable acrylic, epoxy, or polyester resist, or the like, or any other maskant such as identified herein.
  • the layer 14 may be applied by dipping, spray-coating, or electrostatic-depositing to produce a layer thickness of about 0.001-0.010 inch.
  • Selected areas 16 of the layer 14 are then removed to expose portions 18 of the datum surface 12.
  • the use of computer-directed direct laser ablation to generate programmed patterns in the maskant layer 14 allows the application of such patterns to the compound curves of the acetabular cup 4510.
  • a computer-directed laser to directly ablate the maskant or etch resist layer in selected loci is prefe ⁇ ed.
  • the pattern produced by laser ablation is predictable and can be accurately duplicated and repeated from implant to implant.
  • the exposed portions 18 of the surface 12 are etched, preferably using a spray etcher at 100°F spray temperature and 10 lbs/in 2 spray pressure, in a Nitric and Hydrofluoric Acid solution for about 20 minutes. Sufficient "fresh" etchant is continuously impinged upon the etch surfaces 18 to encourage lateral, as well as vertical, etching. It will be understood that alternative etching processes, such as immersing ultrasonics and electrolytic etching, can produce similar results. The etching produces recesses 20 that are undercut, as shown in FIG. 48, and that are, in part, interconnected, as at 22.
  • the metal is etched in such a manner as to deliberately cause undercutting of the pattern, and to permit connection, joining, or "breakthrough" of some of the recesses 20 so as to produce a sharply defined complex network stmcture, including an interconnecting pattern in which the size of most of the recesses 20 is smaller at the surface 12 than at a plane some distance below the surface 12 of the article 4510.
  • the recesses 20 may, in at least some instances, interconnect at and near the surface 12, as at 22 in FIG. 48, to provide enlarged surface recesses 20a (FIG. 49).
  • the etching of the metal surface 12 is thus carried out in one step, wherein non- spherical ovoid-shaped recesses 20 are created, featuring desired sizes and depths that are repeatable from implant to implant.
  • the remaining resist may be removed (FIG. 49) by immersing the body surface 12 in an ND/Phase 23 Stripper bath at about 180°F for about 10 minutes.
  • the maskant layer may be removed by solvation or emulsification.
  • the article 4510 may be lightly post-etched.
  • the implant surface 12 is pressed against the bone B (FIGS. 50 and 51) such that sharp edges 24 of the recesses 20 effect the "scratch fit" with the bone B, which involves shaving off, or milling, particulate segments b of the bone B, which segments b enter the ovoid recesses 20 (FIG. 46) wherein, in due course, the harvested bone segments b stimulate ingrowth of the bone B (FIGS. 52-54) to securely lock the implant to the bone B (FIG. 54).
  • the milling of the host bone B further serves to ream the bone B to the precise size and configuration of the cup 4510, ensuring the best possible fit.
  • the scratch- fit securely adjoins the implant article 4510 to the bone B, to prevent or minimize micro motion between the body 4510 and bone B. The presence of such motion would discourage the ingrowth of bone into the implant and thereby discourage the long-term interconnection of the implant and bone.
  • the scratch-fit application of the implant to the bone harvests bone particulate matter that falls into the surface recesses and is retained by the recesses to encourage and stimulate ingrowth of the bone into the recesses.
  • the recesses are of an ovoid configuration, they provide a greater subsurface fractal area than spherically shaped recesses, and thereby a greater area for engagement of the bone material and the implant.
  • the cup itself can be used as a reaming tool, effecting a perfect fit to the host bone and shortening healing time.

Abstract

Textured surface (12) having micro recesses (20) such that the outer surface overhangs the micro recesses. Embodiments of the textured surface include sharp edges for promoting bone deposition and growth within the micro recesses, protrusions of varying depth from the surface that include overhangs, and micro recesses that are at least partially defined by complex ellipsoids.

Description

TEXTURED SURFACE HAVING UNDERCUT MICRO RECESSES IN A SURFACE
BACKGROUND OF THE INVENTION 1. Field of the Invention
The invention relates to the production of textured surfaces for medical, industrial, and commercial applications and is directed more particularly to surfaces having undercut micro recesses. 2. Description of the Prior Art It is known to use textured surfaces on surgical implants for the purpose of encouraging bone adhesion and thus stabilizing the location of the implant relative to the bone. For example, in an artificial hip, including a femoral sub-assembly for positioning in a patient's femur, and an acetabular sub-assembly for positioning in the patient's acetabulum, the femoral sub-assembly includes an artificial stem which is typically provided with a textured surface, and the acetabular sub-assembly includes an acetabular cup which is typically provided with a textured surface, the textured surfaces being provided to promote bone in-growth.
The desirability of roughened, textured, bone-engaging surfaces to assure stable positioning of surgical implants has been recognized in U.S. Patent No. 5,298,115, issued March 29,1994, in the name of Ian Leonard, U.S. Patent No. 5,456,723, issued October 10, 1995, in the name of Samuel G. Steinemann, U.S. Patent No, 5,603,338, issued February 18, 1997, in the name of Keith D. Beaty, U.S. Patent No. 5,853,561, issued December 29, 1998, in the name of Bruce A. Banks, and U.S. Patent No. 5,965,006, issued October 12, 1999, in the names of Roland Baege et al.
To produce such textured surfaces, one known method is to provide a mass of titanium spheres vacuum fused onto the datum surface of the implant. This method is described in U.S. Patent No. 4,834,756, issued May 30, 1989, to Robert V. Kenna. In a similar procedure, described in U.S. Patent No. 4,644,942, issued February 24, 1987 to Kenneth R. Sump, an extractable component and titanium spheres are densified as a coating, which is fused onto a datum surface of the implant, and the extractable component subsequently is extracted. While an improvement over untreated metal, questions have arisen over the longevity of usefulness of the implanted devices utilizing such surfaces. It is questionable whether there is substantial genuine adhesion. It is believed that the voids formed by the spheres are not sufficient for long-term nourishment of ingrowing tissue and/or bone. Further, there have been failures of prosthetics treated in this manner because of the fusing process adversely affecting metallurgical properties, of the implant material, and because of difficulties in removing manufacturing contaminants, such as cutting oils, from the fused sphere network. Still further, the original datum surface, which can be accurately determined, is lost by the application of the coating spheres. The formation of perforated thin metallic sheets or plates by means of chemical milling and/or photo-chemical etching techniques has been described in U.S. Patent No. 3,359,192, issued December 19, 1967, in the names of Hans- Joachim Heinrich et al., U.S. Patent No. 5,606,589, issued February 25, 1997, in the names of Anthony J. Pellegrino et al., and U.S. Patent No. 5,814,235, issued September 29, 1998, in the names of Anthony J. Pellegrino et al. The processes therein described have been found lacking in precise control over the degree and extent of roughness or texturing.
An acetabular cup is a hemispherical device that is implanted in the acetabulum in hip-replacement surgery. The cup serves as a "socket" in a ball-and-socket joint of the hip. Generally, a lining in the cup consists of a biologically inert anti-friction bearing surface, such as high molecular weight polyethylene. The external portion of the cup is usually made of a biocompatible metal, such as cobalt-chromium or titanium alloys that have the stiffness needed to support the bearing surface, and the dimensional stability needed to prevent deflection or displacement of the bond formed to the surface of the host bone. A strong mechanical bond to the bone is needed because, in use, the joint is subjected to strong mechanical forces. Commonly, the exterior of the cup is textured by diffusion bonding metal spheres so as to form a complex network on the exterior surface, in hopes that bone ingrowth will generate a mechanical bond. Some manufacturers machine patterns of grooves in these surfaces. Because of metallurgical annealing in the fusion process, and limitations in machining, the surfaces so generated have not been optimal and have not reached the desired installed-life duration. When the cup is installed, an accompanying reamer is furnished to machine the bone surface to close dimensional fit to the replacement device.
Accordingly, there is a need for an acetabular implant having an improved exterior surface that effects a short-term bond with the bone to which the implant is affixed, and that provides for long-term increased bonding between the implant and the bone, and that further requires no reamer or other bone-machining device.
SUMMARY OF THE PREFERRED EMBODIMENTS A preferred embodiment of the invention is a textured surface which is adapted to interlock with an adjacent body and method of producing a textured surface.
A further embodiment is to provide a texture having an undercut micro recesses in a surface of a body and method of producing a textured surface.
A still further embodiment provides recesses in a desired pattern which is measurable and predictable, and which can be duplicated and repeated precisely in any selected number of surfaces and method of producing a textured surface.
A still further embodiment is a surgical implant device wherein the material of the device retains its metallurgical properties throughout production and method of producing a textured surface.
A still further embodiment is a surgical implant, with a textured surface that promotes the in-growth of tissue and/or bone to securely interconnect the implant and the tissue and/or bone and method of producing a textured surface.
A still further object is to provide an implant with surfaces that include undercut and interconnecting recesses which promote and facilitate ingrowth of bone and which, upon implantation, facilitate a "scratch fit" with bone, to stabilize the position of the surface on the bone and to initiate an interconnection process between the implant and the bone. The "scratch fit" is accomplished by the textured surface scraping bone from the implant site during a press fit implantation, thereby producing autografted bone in the voids of the textured surface.
A still further embodiment is a surgical implant for attachment to tissue (e.g., bone). A still further embodiment is a surgical implant for attachment to bone. A still further embodiment is a surgical implant facilitating bone harvesting and seeding of the surgical implant with particulate bone matter during attachment of the implant to the bone.
A still further embodiment is a surgical implant which exhibits a precise fit with a bone implant site, to reduce micro-motion between the implant and the bone site.
A still further embodiment of the invention is to provide a surgical implant having undercut micro recesses with sharply defined edges in a bone-engaging surface thereof.
Yet another embodiment of the invention is the provision of an article, having a surface that includes a multiplicity of undercut microrecesses in the surface, such that the article thereby exhibits a greater fractal area at a level below the surface than is exhibited at the surface, the article produced by a method comprising the steps of applying a maskant layer to substantially an entirety of the article surface, removing the maskant layer in selected loci to expose underlying portions of the article surface in a selected, predictable, and reproducible pattern, applying an etchant to the exposed underlying surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce a multiplicity of undercut recesses, and removing the remaining maskant layer portions to provide the article surface in exposed condition with the multiplicity of recesses undercut and comprising interconnected recesses, to provide an engineered pattern of the recesses. There is, furthermore, an article having a multiplicity of undercut micro recesses in a surface thereof, the recesses being in a selected pattern which can be repeated in any selected number of surfaces and produced by a method having the steps of: applying a maskant layer to substantially an entirety of a selected surface of the article; removing the maskant layer by computer-directed laser ablation in programmed loci to expose underlying portions of the surface of the article in a programmed pattern; applying an etchant to the exposed underlying surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce the multiplicity of undercut recesses; and removing the remaining maskant layer to provide the selected surface in exposed condition with the multiplicity of undercut recesses therein. In accordance with a still another embodiment of the invention, there is provided a surgical implant having facility for stimulating ingrowth of bone upon attachment of the implant to a bone that is produced by a method that includes the steps of: providing a rigid article; applying a maskant layer to substantially an entirety of a datum surface of the article; removing portions of the maskant layer in selected loci to expose underlying portions of the surface of the article; applying an etchant to the exposed underlying surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce a multiplicity of undercut recesses having sharp edges at their intersections with the datum surface; and removing the remaining portions of the maskant layer to provide the datum surface in exposed condition with the sharp edges for shaving particulate matter from the bone, and with the recesses for receiving and retaining the bone particulate matter for stimulating ingrowth of bone.
In accordance with a still further embodiment of the invention, there is provided a textured surface in a surgical implant produced by a method that includes the steps of: applying a maskant layer to substantially an entirety of a datum surface of the implant; removing portions of the maskant layer in selected loci to expose underlying portions of the datum surface of the implant; applying an etchant to the exposed underlying datum surface portions for a time sufficient to etch the exposed surface portions and to enable the etchant to etch beneath remaining portions of the maskant layer and produce a multiplicity of undercut recesses having sharp edges at their intersections with the datum surface; and removing the remaining portions of the maskant layer to provide the datum surface in exposed condition with the sharp edges for shaving particulate matter from the bone, and with the recesses for receiving and retaining the bone particulate matter for stimulating in-growth of bone.
In accordance with a still further embodiment of the invention, there is provided a surgical implant that is attached to a bone, in accordance with a method comprising the steps of: providing a surgical implant having a datum surface, a multiplicity of micro recesses in the datum surface, and bone milling structure on the datum surface; pressing the datum surface against a surface of the bone; and urging the implant along the bone surface to mill particulate bone matter from the bone, wherein the recesses receive and retain the particulate bone matter to stimulate ingrowth of the bone into the datum surface. In accordance with a still further embodiment of the invention, there is provided a surgical implant having a datum surface and a multiplicity of undercut microrecesses in the datum surface, such that the implant exhibits a greater fractal area at the level below the datum surface than is exhibited at the datum surface, intersections of the datum surface and the recesses defining sharp edges; pressing the datum surface against a surface of the bone, and urging the implant along the bone surface, to cause the sharp edges to shave particulate bone matter from the bone, wherein the recesses receive and retain the particulate bone matter to stimulate ingrowth of the bone to attach the surgical implant to the bone.
In accordance with a still further embodiment of the invention, there is provided a method for bone harvesting and seeding of a surgical implant with particulate bone matter during attachment of the implant to the bone, the method comprising the steps of providing a surgical implant having a surface for engagement with a bone surface, the implant having a multiplicity of undercut micro recesses and bone milling structure in the surface thereof, wherein moving the implant along the bone, such that the milling structure dislocates particulate bone matter from the bone, the bone matter falling into the micro recesses and retained thereby to stimulate ingrowth of the bone into the undercut recesses harvests the bone and seeds the surgical implant with particulate bone matter during attachment of the implant to the bone.
In accordance with a still further embodiment of the invention, there is a surgical implant having generally opposed datum surfaces spaced from each other by a predetermined distance, each of the datum surfaces being adapted to interlock with a bone surface that is made by a process comprising the steps of providing an article having first and second datum surface portions adapted to respectively engage first and second bone surfaces, the datum surface portions being spaced from each other by the predetermined distance which is substantially equal to a distance between the first and second bone surfaces; applying a maskant layer to substantially an entirety of each of the datum surfaces; removing the maskant layers in selected loci to expose underlying portions of the datum surfaces in a selected pattern; applying an etchant to the exposed underlying datum surface portions for a time sufficient to etch the exposed portions of the datum surfaces and to enable the etchant to etch beneath the remaining maskant layers and produce undercut recesses; and removing the remaining maskant to provide the opposed datum surfaces in exposed condition with the multiplicity of undercut recesses and devoid of structure protruding therefrom.
In accordance with a still further embodiment of the invention, there is provided a surgical implant comprising an article having a datum surface for abutting engagement with a bone, and a multiplicity of undercut micro recesses in the datum surface, such that the body exhibits a greater fractal area at a level below the surface than is exhibited at the surface.
Intersections of the recesses and the datum surface define sharp edges adapted to cut the bone and produce bone particulates. The recesses are adapted to receive and retain the bone particulates cut from the bone by the edges, to stimulate ingrowth of the bone into the recesses. For all objects of the invention that describe a device or a structure, the invention includes a method for producing the described devices or structures.
The above and other embodiments of the invention, including various novel details of components and method steps, will now be more particularly described with reference to the accompanying drawings and pointed out in the claims. It will be understood that the particular methods and devices embodying the invention are shown and described by way of illustration only and not as limitations of the invention. The principles and features of this invention may be employed in various and numerous embodiments without departing from the scope of the invention. A further object of the invention is, therefore, to provide an acetabular cup having an outer bone-engaging surface provided with a multiplicity of sharp-edged undercut recesses for receiving bone particulates milled from the bone by the sharp edges during the mounting
of the cup.
A further object of the invention is to provide a method for attaching such acetabular cup to a host bone.
With the above and other objects in view, a feature of the invention is the provision of an acetabular implant having a datum surface for abutting engagement with a bone, and a multiplicity of undercut micro recesses in the datum surface, such that the body exhibits a greater fractal area at a level below the surface than is exhibited at the surface. Intersections of the recesses and the datum surface define sharp edges adapted to cut the bone and produce bone particulates. The recesses are adapted to receive and retain the bone particulates cut from the bone by the edges, to stimulate ingrowth of the bone into the recesses.
In accordance with a further feature of the invention, there is provided a method for attaching an acetabular orthopedic surgical implant to a host bone. The method comprises providing an acetabular cup having a datum surface, a multiplicity of micro recesses in the datum surface, and a bone-milling structure on the datum surface, pressing the datum surface against a surface of the host bone, and urging the implant along the host-bone surface to ream the host bone and to mill particulate bone matter, from the host bone. The recesses are adapted to receive and retain the particulate bone matter which stimulates ingrowth of the host bone.
The above and other features of the invention, including various novel details of components and method steps, will now be more particularly described with reference to the accompanying drawings and pointed out in the claims. It will be understood that the particular methods and devices embodying the invention are shown and described by way of illustration only and not as limitations of the invention. The principles and features of this invention may be employed in various and numerous embodiments without departing from the scope of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS Reference is made to the accompanying drawings in which are shown illustrative embodiments of the invention, from which its novel features and advantages will be apparent. In the drawings:
FIG. 1 is a diagrammatic sectional view of an article having a surface in which it is desired to provide a multiplicity of undercut micro recesses;
FIG. 2 depicts the article of FIG. 1 with a layer of maskant material deposited on the aforesaid surface;
FIG. 3 depicts the article and maskant layer of FIG. 2 with the maskant layer in part removed;
FIG. 4 is similar to FIG. 3 and showing portions of the article not covered by maskant etched away to provide undercut and interconnected recesses; FIG. 5 is similar to FIG. 4, but showing the remaining maskant layer stripped away; FIGs. 6-10 are progressive diagrammatic sectional views showing positioning of the article adjacent a bone and interconnection of the article and the bone;
FIG. 11 is a diagrammatic sectional view of a surgical implant having a plurality of surfaces treated as illustrated in FIGS. 2-10; FIG 12 is a diagrammatic sectional view of structural features of the a surface texture;
FIG 13 is a three-dimensional illustration of a textured pattern; FIG 14 is a diagrammatic sectional view of a complex ellipsoid; FIGs. 15a- 15c illustrate diagrammatic sectional views off structural features of a textured surface; FIG. 16 is a diagrammatic sectional view of a complex ellipsoid;
FIG. 16A is a diagrammatic sectional view showing an embodiment of complex ellipsoids with an oblique orientation;
FIG. 16B illustrates an exemplary textured structure;
FIG. 16C - 16D are diagrammatic sectional views of a textured structure being inserted into a bone channel;
FIGs. 17A - 17E are three-dimensional illustrations of exemplary textures; FIGs. 18 - 27 are diagrammatic cross-sectional views of successive stages in the making of a mesh-and-plate implant in accordance with an embodiment of the invention;
FIG. 28 is a top plan view of a mesh-and-plate implant made in accordance with the method illustrated in FIGs. 18-27;
FIG. 29 is similar to FIG. 28, but illustrative of an alternative implant; FIG. 30 is an enlarged illustration of the mesh portions of the implants of FIGs. 28 and 29;
FIG. 31 is a three-dimensional illustration of a textured implant; FIG. 32 is a diagrammatic cross-section of an implant; FIG. 33 is an illustration of an implant with protrusions; FIG. 34 is a diagrammatic cross-sectional view of an implant with protrusions; FIG. 35 is a diagrammatic cross sectional view of a textured implant; FIG. 36 is a diagrammatic cross sectional view of an implant with recesses; FIGs. 37A-37C illustrate implants with apertures;
FIGs. 38A-38D illustrate implants with ribs;
FIGs. 39A - 39C are diagrammatic cross-sections illustrating textured implants; FIG. 40 illustrates a two dimensional pattern of the present invention; FIG. 41 is a diagrammatic illustration of a barbed implant; FIG. 42 A is a diagrammatic cross-sectional illustration of an implant having a directionally impinged textured surface; and
FIG. 42B is a diagrammatic cross-sectional illustration of an implant having a non- directionally impinged textured surface.
FIG. 43 is a side elevational view of a hip replacement assembly, including an acetabular cup illustrative of an embodiment of the invention;
FIG. 44 is an exploded perspective view of the assembly of FIG. 43; FIGS. 45-49 are progressive diagrammatic sectional views illustrating a method for making an acetabular cup datum surface having undercut micro recesses; and
FIGS. 50-54 are progressive diagrammatic sectional views showing positioning of the acetabular cup adjacent a bone, reaming of the bone, and interconnection of the cup and the bone.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Undercutting occurs, for example, when the chemical etchant removes metal beyond the boundary of a maskant, or resist layer. Often, such undercutting limits the fine resolution needed for many processes, such as the production of electronic devices, rotogravure plates, and other fine parts. However, predetermined and controlled undercutting may be exploited and utilized to produce useful and novel three-dimensional geometries by allowing the undercutting effect to expand deeper regions of a chemically applied pattern, so that the resulting treatment layer is an engineered pattern of undercut recesses. This provides sharp geometries when desired, and produces a higher void volume and larger fractal dimensions than are obtainable by other methods. Further, it permits retention of a predetermined area of original surface to afford an engineered and repeatable "datum surface," or surface intended to abut another body to which the undercut surface will be attached. The metal of the complex pattern is identical and contiguous with the base metal of the treated body, because it is generated in the body, and not later applied, such as the fused metal spheres mentioned hereinabove.
While the methods and products described herein are described in terms of producing textured metal surfaces, and while it is expected that the method will find substantial utility in metal bodies, and while the method produces deeply textured surfaces in metals, such as titanium, zirconium, stainless steel and alloys thereof, tantalum, refractory metals, metal carbides, oxidized zirconium and cobalt/chromium, it will be appreciated that the method is readily adapted for use with bodies of other materials including ferrous and non-ferrous metals, and alloys thereof, and ceramics, plastics and glass, and composites of metals, ceramics, plastics, and glass or any other material. Application of the present invention is particularly useful in materials that are susceptible to so-called "nick-bend failures" or "notch failures." An example of a notch failure is crack propagation in metal surfaces. Such propagation is known to occur, for example, in materials having an applied surface texture. An example of a testing method for the measurement of creep crack growth rates in metals is provided in ASTM Standard El 457- 00, which is herein incorporated by reference in its entirety. One material that is particularly suited for implant applications is titanium. The susceptibility of titanium to crack propagation is well documented. Annealing is one method to relieve strain from a material surface such as titanium. Annealing, however, can have other deleterious effects on metals (e.g., increased softness). Another documented method for mitigating nick-bend failures is to strain relieve the material by, for example, removing the "rind", "skin" or outer surface of the metal that has been strained. Examples of techniques for removing rind includes machining, grinding, laser welding or laser machining involving thermal shock and sudden phase changes. These techniques may be employed to expose the pristine metal beneath the surface. In some cases, however, removing the rind from a textured surface has the unwanted effect of removing a portion of the texture. For example, where lasers are used to machine a metal (e.g., applying a texture to a surface using laser etching techniques), there is created an area of increased strain where the laser acted upon the surface of the material. One technique for strain release of that affected area is to remove the surface of the material. Where laser machining was performed for the purpose of applying a texture, removing that affected area would, in some cases, reduce or eliminate the effectiveness of the texture.
The methods and products of the present invention avoid this problem. To the extent that the laser ablation of maskant has a deleterious effect on the material being treated, in one embodiment of the invention, those effects are minimized or eliminated during the etching process resulting in a strain-reduced/relieved textured surface. That is, the strained regions of the surface are etched-away to relieve the strain, without forming a non-strained region.
Furthermore, it has been found that strained metal (such as where a laser has been applied to a surface) tends to etch, corrode or dissolve faster than metal in its pristine state. In a preferred embodiment, the laser ablation of maskant (e.g., to expose the surface of the metal for later etching) increases localized strain on the surface of the metal, thereby focusing future etching to produce a precisely textured strain-relieved surface. Furthermore, it has been found that the strained areas etch somewhat more quickly thereby promoting the preferentially accelerated resolution of these strains.
In preferred embodiments, the textures described herein are useful in the medical, industrial, consumer product, computer, electrical, and mechanical fields. For example, in the medical field, textures are useful in orthopeadic implants (e.g., in artificial hips, knees, acetabular cups, ankles, shoulders, and interbody fusion devices); spinal implants (e.g., spinal fusion devices, articulating intravertebrae devices, and external spinal fixation devices); neurocranial and maxillofacial implants (e.g., fracture plates and mesh, scafolds, and bridges); dental implants (e.g., osseointegration posts); joint replacement implants, cemented and cementless applications, and any medically implanted device where there is a need for improved fixation. Such improved fixation is useful between metal to tissue (e.g., bone), metal to plastic, metal to adhesive, soft tissue to bone, ligament to bone, soft tissue to implant, positional stability of implant (e.g., rough surface to hold implant in place during a surgical procedure) and for providing increased vascular flow (e.g., textured surface provides space between the implant and bone to allow for greater vascular flow between bone and implant).
In other fields, textures have use in any component device in which a material requires a surface conditioning to promote adhesion or increase friction. Exemplary fields include aerospace (e.g., fusilage bonding and fasteners); automotive (e.g., brake shoes to brake pads), sports gloves (e.g., rock climbing, football and golf gloves), composites (e.g., golf club heads, and any other contact surfaces where increased grip is desired), and tool sharpening. Other applications in industry and manufacturing will be apparent for the textured pattern of the present invention, including cutting surfaces (e.g., rasps, dental drills, medical files, burrs and orthopeadic cutters). Further utility will be found where improved adhesion is desired (e.g., metal to metal adhesion, polymer to polymer adhesion, metal to polymer adhesion, and on layers of material that are laminated to one another).
Among the characteristic features of the present invention are engineered patterns (e.g., application specific custom patterns and textures, repetitive or random patterns, patterns created on complex geometries, with no metallurgical changes in material, a chemically pure resulting surface, and a pattern that is integral with the parent material (e.g., not a coating). Application of these features achieves exemplary benefits such as: precise control of micropore size, accurate maintenance of a percentage of original surface; reduction of micromotion, and/or retention of bone chips shaved from undercut edges in texture pockets. Referring to FIG. 1, it will be seen that there first is provided an article 10 of one of the above-mentioned materials, or a material similar thereto. The article 10 is provided with a datum surface 12 in which it is desired to provide a multiplicity of undercut recesses.
As shown in FIG. 2, a layer 14 of maskant material is deposited on substantially the entirety of the surface 12. The maskant is a suitable acrylic, epoxy, or polyester resist, or the like. The layer 14 may be applied by dipping, spray coating, or electrostatic depositing, or any other coating method to produce a layer thickness of about 0.001-0.010 inch. The coated article of FIG. 2 preferably is baked at 200°F (±10°F) for about 15-17 minutes, or any sufficient combination of time, pressure (such as vacuum-baking) and temperature to insure the removal of water, as is customarily used in the art. Kodak Thin Film Resist® has been found to be a quite suitable maskant. To the Kodak Resist is added 2%, by weight, carbon black pigment, or other pigment described hereinbelow.
In one embodiment, the adhesion of the resist or masking agent to a metal surface of the object to be textured preferably includes of an actual chemical, ionic, or molecular bond to the metal itself. In one embodiment, the undercutting process preferably is conducted via spray impingement of the etchant, or other agitation, such as turbulence or ultrasonic cavitation, often for periods of time that are more prolonged than is generally encountered in common photo fabrication. The duration of the undercutting process is dependant upon the substrate selected and the etchant system chosen. Preferably, etching lasts up to 10-15 minutes. It may exceed 20 minutes. In some embodiments of the present invention use a layer 14 of common photopolymerized polyester resist, requires cleaning and abrading of the datum surface prior to application of layer 14. As is common good practice in the metal finishing field, in some embodiments, pre-etching and pre-baking of the metal surface is sometimes required to insure the integrity of the maskant-metal bond. In one embodiment, it is desirable to remove a minute amount of surface material (preferably 0.001 inches to 0.005 inches) to insure a chemically clean and pristine metal surface. Additional embodiments include the use of a layer 14 of epoxy dip coatings, electrostatic coatings, electrophoresis coatings or other electro-deposited coatings, and spray coatings of resist or masking agents.
Dispersing an appropriate pigment or dye into a maskant layer can render the maskant laser receptive. The maskant is selected based on the wavelength of the laser, or any projected light source, to be used to produce the desired pattern of maskant 14 on surface 12. In one embodiment, in the case of an infrared laser, the resulting local heating from the absorption of laser energy selectively removes tiny areas of the resist or maskant layer 14, thereby exposing the underlying metal surface 12 of the article to the action of an etchant. Ordinary conventional photographic image and development techniques may be used with these photosensitive materials and methods. They are less suitable, however, for contoured parts, as artwork negatives cannot easily be laid upon them for exposure.
As noted above, a preferred maskant is Kodak Resist, to which is added about 2% carbon black pigment, or other pigment more particularly suited to the laser wavelength to be employed. The pigment is dispersed into the maskant in a high shear mixer until fully dispersed, or until a temperature rise of 15-20°C is reached. The resulting maskant is applied by dipping or by spraying, spinning, brushing or electrostatically depositing onto the surface to be treated.
Selected areas 16 of the layer 14 are then removed to expose portions 18 of the datum surface 12. In one embodiment, the use of computer-directed direct laser ablation to generate programmed patterns in the maskant layer allows the application of such patterns to irregularly shaped finished goods, parts, or items which have surfaces of compound curves or radii. Such shapes are routinely encountered in implantable medical devices, such as dental post implants, hip joint assemblies, and maxillofacial prosthetics.
To generate a selected image, or array of recesses, or a fractal pattern, in a laser receptive maskant, the use of a computer-directed laser to directly ablate the maskant or etch resist layer in selected loci is preferred.
FIG. 40 illustrates a preferred two-dimensional pattern 410. In one embodiment, the pattern is transferred to the surface maskant by laser ablating black regions 412. The black regions 412 are then etched with undercutting until the etched regions reach the desired complex 3-dimensional arrays of cavities. In one embodiment, the resulting patterns does not superficially resemble the starting pattern, though the resulting pattern is a derivative of the starting pattern, and/or the starting patterns basic fractal elements.
In a preferred embodiment of the method, ablations are made by direct writing with a neodymium-doped YAG laser with a wavelength of 1.06 microns, to which carbon black is receptive. A pattern is selected which optimizes the effects of undercutting. The pattern chosen is saved in Tagged Image File Format (TIFF) or as a plot (PLT) graphics file, and used to direct a laser marker.
In one embodiment, an Electrox, Scriba Nd:YAG laser marker may be used, with patterns stored in digital file format. Upon laser exposure, the underlying surface portions 18 are exposed in those areas in which the maskant absorbs the laser beam. The pattern produced by laser ablation is predictable and can be accurately duplicated and repeated from implant to implant. While the aforementioned YAG laser has been found effective in the present invention, so also have CO2, diode pump, and green lasers. Any laser capable of ablating, or thermally vaporizing, the maskant to generate a desired pattern of exposed surface may be used in carrying out the method described herein. Other methods of removing maskant include: mechanical tools, chemical milling, photo-chemical etching and laser eradication.
The pattern can be generated on a Computer Aided Design (CAD) system using any compatible file type, or generated as a phototool for imaging. The pattern can be scanned from a drawing, print, photograph, or the like, and converted into any file type compatible with the laser system employed.
An alternative method of manufacture is to use a photo sensitive maskant, which is applied to the device as stated above, or applied as a dry film which is laminated to the surface. The maskant is then exposed, using a light source of an appropriate wavelength (typically 280-550 nanometers). Portions of the maskant are cross-linked and/or bonded to the surface during the exposing process (in the case of negative working resist). The other areas of the maskant are dissolved or washed away in a developing process that utilizes a compatible developer solution, such as sodium or potassium carbonate, or stoddard solvents, thereby exposing the underlying material. The exposed portions 18 of the surface 12 are etched, preferably using a spray etcher at 100°F spray temperature and 10 lbs/in spray pressure, in a Nitric and Hydrofluoric Acid solution for about 20 minutes. Sufficient "fresh" etchant is continuously impinged upon the etch surfaces 18 to encourage lateral, as well as vertical etching. It will be understood that alternative etching processes, such as immersing ultrasonics and electrolytic etching, can produce similar results. In one embodiment of the present invention, the methods of replenishing the etchant at the surface being textured is required to successful practice of the invention. At the etchant/metal interface a depletion condition exists as some of the active species in the etchant are consumed by the etching action and the formation of metal salts. Because aggressive and uniform etching action is preferable to ensure development of the desired elliptical geometry of the etched cavity, a spray impingement method is frequently used. In one embodiment, such a spray method allows an off-axis or directional control to achieve the resulting textured surface and causes the undercutting to be in one or more desired directions or axes of the part (e.g., device 10) rather than another. In a prefeπed embodiment, the spray etching system can be arranged so as not to impinge from all angles, or not to rotate with respect to the workpiece. For example, if a spray nozzle is affixed so as to impinge the work at a constant oblique angle to the piece being etched, then surface flow effects will control the etching process in the microscopic regions of the ablated maskant in such a way that "tilting" of the etched cavities (described in more detail below) is a consequence of the process.
The etching produces recesses 20 which are undercut, as shown in FIG. 4, and which are, in part, interconnected, as at 22. In the prefeπed embodiment, the metal is etched in such a manner as to deliberately cause undercutting of the pattern, and to permit connection, joining, or "breakthrough" of some of the recesses so as to produce a sharply defined complex network structure, including an interconnecting pattern in which the size of most of the recesses is smaller at the surface 12 than at a plane some distance below the surface 12 of the article 10. The recesses 20 may, in at least some instances, interconnect at and near the surface 12, as at 22 in FIG. 4, to provide enlarged surface recesses 20a (FIG. 5).
The etching of the metal surface 12 is thus carried out in one step, as opposed to repetitive etching suggested in some of the prior art references cited hereinabove. In the prefeπed one-step etching process, non-spherical ovoid shaped recesses are created featuring desired sizes and depths which are repeatable from implant to implant.
The remaining resist may be removed by immersing the body surface in a NJ/Phase 23 Stripper bath at about 180°F for about 10 minutes. Alternatively, the maskant layer may be removed (FIG. 5) by solvation or emulsification. If desired, the article 10 may be lightly post-etched.
In one embodiment, in a titanium hip joint, for example, the metal was first washed with an alkaline degreasing detergent (e.g., an Oaktite® solution), water-rinsed in de-ionized water and briefly pre-etched in a hydrofluoric/nitric acid etchant solution, so as to produce a chemically clean, freshly-exposed metal surface suited to maskant adhesion, water-rinsed again thoroughly, and oven dried at 110°C prior to coating with the selected resist agent (e.g., Kodak KPFR, or any other resist, including other polymer classes, such as reactive epoxy or urethan systems, or lacquers and varnishes). A polyester resist coating was then applied by dipping, air-drying for 15 minutes, and baking at 100°C for 20 minutes. Alternatively, an epoxy e-coating (e.g., PPG Powercron® CF-665) can be successfully used. A desired pattern may then be laser-imaged onto the surface with a 90 watt neodymium- doped YAG laser at 85% power, and at a machine setting of 3 frequency units to achieve a shallow penetration to and below the surface of the base metal. The typical depth of penetration is 10 microns. This assures the cleaning of the metal base layer to remove maskant ablation residues from the regions to be etched. The hip joint was then again baked at 100°C prior to etching to insure full cross-linking of the polymer, and to remove low- molecular-weight pyrolysis products from the maskant polymer.
The surface of the hip joint was then etched to the desired depth. The broadest depth range is 0.1mm to 2mm, with a prefeπed depth range of 0.4 to 0.6 mm. Certain patterns may, in extreme situations on some metals require shallower or deeper etching than the prefeπed range, in order to develop a desired three-dimensional pattern. For example, more delicate pattern designs, may require very light etching in order to preserve the original pattern details. However, nearly all the patterns used to date have been well-formed by etch depths of 0.4 to 0.6 mm. The depth range preferably depends on pattern coarseness. In one embodiment, coarser patterns have wider land areas (discussed below), and therefore can tolerate deeper etch depths before they are cut off by undercutting in a vertical spray etcher at 20 to 30 minutes (depending on desired depth and pattern coarseness) at 100°F.
After etching to the desired depth the article is rinsed well in running water and air dried. The article is then inspected for proper etching, sufficient undercutting, and general quality. The resist or maskant was then stripped from the hip joint using a nuphase stripper solution such as a concentrated caustic stripping solution (e.g., Oakite® Eurostrip® 704 manufactured by PC&E), at a temperature of 160°F, for 15 minutes. After stripping, the article was rinsed in deionized water and oven dried at 220°F. In one embodiment, there is thus provided a method for producing a complex, at least in part interconnecting pattern, or similar 3-dimensional surface treatment, to enhance the attachment of biological matter to a surface of an implantable device, or the interconnection of other bodies to be bonded, made by selective etching and undercutting of a surface so as to form a network of at least in part interconnected recesses. The pattern is formed by the direct laser ablation of an etch resist or maskant layer, allowing the textured surface to be applied to items with complex or curved surface geometries. The pattern is stored in a CAD or other computer-based system which controls the maskant ablations and is predictable and subject to repetitive duplication. The article is chemically etched to form the complex pattern. The metallurgical properties of the material of the article are not altered by heat, but remain substantially consistent during the process. Soft tissue or bone may in-grow the surface so produced, resulting in an interpenetrating network that offers superior mechanical adhesion and resistance to degradation. Further, the sharp edges at the intersections of the undercut recesses and the original datum surface facilitate an initial "scratch- fit" between the implant surface and a bone. In operation, to produce a textured surface on a surgical implant, a selected pattern of undercut and at least in part interconnected recesses is effected in a surface of the surgical implant (FIG. 5). In implantation, the implant surface 12 is pressed against the bone B, (FIG. 6) such that sharp edges 24 of the recesses effect the "scratch fit" with the bone B, which involves shaving off, or milling, particulate segments b of the bone B, which segments b enter the ovoid recesses 20 wherein, in due course, the bone segments b stimulate in-growth of the bone B (FIG. 7) to securely lock the implant to the bone B (FIG. 8).
Thus, the scratch-fit securely adjoins the implant article 10 to the bone B, to prevent or minimize micro motion between the body 10 and bone B. The presence of such motion would discourage the ingrowth of bone into the implant and thereby discourage the long-term interconnection of the implant and bone.
Further, the scratch-fit application of the implant to the bone harvests bone particulate matter which falls into the surface recesses and is retained by the recesses to encourage and stimulate ingrowth of the bone into the recesses. Inasmuch as the recesses are of an ovoid configuration, they provide a greater sub-surface fractal area than spherically shaped recesses, and thereby a greater area for engagement of the bone material and the implant.
Referring to FIG. 11, it will be seen that for bones B accepting an implant 10 having a plurality of datum surfaces 12, including opposed surfaces 12a and 12b, the accurate location of the datum surfaces is most critical, inasmuch as any build-up of implant material above the datum surfaces causes the implant not to be accepted by the bone B. Texturing the surfaces 12 below the surfaces 12 does not add material to surfaces 12. Whereas, texturing the surfaces 12, by adding texture above the surfaces increases the space required between the opposed bone surfaces to accept the implant and leads to rejection of the implant. Known methods of texturing by adding to a surface lack the required precise control to determine the deviation of the peaks of the added material. The method presented herein facilitates accurate and precise location of datum surfaces of surgical implants.
The milling of the host bone B may further serve to ream the bone B to the precise size and configuration of the article 10, insuring the best possible fit. Accordingly, appropriately shaped and sized buns of the texture on article 10 are preferably furnished to pre- form a receptacle in the bone to properly receive the article 10. The scratch-fit securely adjoins the implant article 10 to the bone B, to prevent or minimize micro motion between the implant 10 and bone B. The presence of such motion would discourage the ingrowth of bone into the implant and thereby discourage the long-term interconnection of the implant 10 and bone B.
In some embodiments, a device with a textured surface according to the present invention, can affect a self-fitting function. For example, it will be appreciated that where a textured surface, according to the present invention, is applied to an acetabular cup, the cup itself can be used as a reaming tool, effecting a perfect fit to the host bone and shortening healing time. Further, in the process of self- fitting, there is milled, or harvested, fine bone particulates, or pulp, from the patients' own body, for example, as shown in FIGS. 6-10. The resulting material is forced into the recesses to serve as a nucleation host for a spontaneous homograft completed by the attraction and growth of the patient's osteoblasts, providing a strong bond and longer installed lifetime.
Some embodiments of the present invention may incorporate sharp-edged geometry such as at undercut 3 (See FIG. 12). It may be desirable for the sharp-edged undercut geometry to be later modified by a subsequent dulling process so as to causes sharp edges to be rounded. For example, abrasive blasting, glass bead blasting, or a subsequent acid etch all may be used to slightly dull or "break" the original sharp edges, if desired. Such a subsequent dulling process may include, for example, etching, polishing (e.g., electropolishing), abrasive reduction, buffing, and honing. Through this process, at least some of the walls 7 (shown on Fig. 14 and described in more detail below) may become perpendicular to the surface of the article, or may actually diverge outward from each other as they approach the surface of the texture pattern. In some embodiments, post-processing (e.g., cleaning or polishing) defeats the benefits of the textured surface. Still, some practitioners may incorporate a post-processing step. Looking in more detail at formed features according to some exemplary embodiments of the present invention, FIG. 14 illustrates a prefeπed geometry of a cavity 20 which has been deliberately produced with the geometry of a complex ellipsoid. A complex ellipsoid is preferably derived from two or more ellipsoids. In a prefeπed embodiment, the complex ellipsoid is derived from at least two non-spherical ellipsoids. Alternative embodiments may include combinations of spherical and non-spherical ellipsoids. The complex ellipsoids may be a combination of ellipsoid 30a and ellipsoid 30b. The complex ellipsoids may alternatively combine three or more ellipsoids with three or more different angular projections. More particularly, a geometric shape of the illustrated cavity 20 may be described as being defined, at least in part, by two non-spherical ellipsoids sharing a major axis 9 and having varying angular projections (e.g., an ellipse having a 40 degree protection, superimposed on an ellipse having a 50 degree projection, or any combination of ellipses from about 9 degrees to about 89 degrees so as to produce a species of the complex ellipse shape).
Ellipsoid 30b with a narrower angular projection defines a bottom 4 of cavity 20. Ellipsoid 30a with a wider angular projection defines an arched undercut 3 which is contiguous with wall 7 and bottom 4. In the prefeπed embodiment wall 7 and bottom 4 are concave and contiguous. Cavity 20 (FIG. 16) may be further characterized as having a ratio of cavity width, w, to cavity depth, d, that is greater than or equal to unity. The preferable width:depth ratio ranges from 1:1 to 9:1. In a prefeπed embodiment, the ratio is approximately 4:1.
Referring now to FIGs. 12, 14, 15a, 15b, and 15c, protrusions 2a, 2b, and 2c have differing geometries each of which is preferably defined by the relationship between at least two complex ellipsoids. Protrusions 2a, 2b, and 2c extend from bottom surface 4 of cavity 20 toward datum 12. Protrusion 2a has a peak 5a in the form of a plateau or mesa which is coincident with outer surface 12. Complex ellipsoids 1 la and 1 lb define the lateral dimensions of protrusion 2a. Cavity 20 is also defined by complex ellipsoids 11a and l ib which intersect datum 12 to create cavity 20 in outer surface 12. The portion of outer surface 12 remaining untouched by the ellipsoids 1 la, 1 lb defines peak 5a. An ellipsoid forming protrusion 2a preferably forms an undercut 3 at the face of the protrusion. Protrusion 2c has a sub-peak 5c located between datum 12 and bottom 4. Sub-peak
5c is defined by the intersection point of at least two complex ellipsoids 11. In a prefeπed embodiment, protrusion 2c is formed from the at least two complex ellipsoids 1 la, 1 lb, which overlap to the extent that no overhang is created in wall 7 of protrusion 2c. In some embodiments the overlapping of ellipsoids may result in an overhang on one face of the protrusion but not on another face of the same protrusions.
Protrusion 2b has an intermediate peak 5b which is also located between datum 12a and bottom 4. Intermediate-peak 5b is preferably defined by two or more complex ellipsoids 11a and 1 lb that do not overlap. The complex ellipsoids 11a, l ib that at least partially define intermediate-peak 5c, however, are in close enough proximity to each other that the portion 140 of article 10 that previously existed between intermediate-peak 5c and datum 12a can be predicted to break-off during manufacture such as, for example, during polishing of the etched product, leaving an intermediate peak 5c. In one embodiment, the surface is "softened" by common buffing or polishing methods (as described above). Thus, in one embodiment, the surface is modified such that the sharp edges will be removed, as well as some of the tops of the proj ections .
For clarity, FIGS. 14 and 16 shows the major axis 9 substantially parallel with datum surface 12. Orientation of the major axis may vary from perpendicular to parallel depending on the desired finished texture, the pattern of the desired texture and direction of the texture. Prefeπed embodiments have an orientation of axis 9 that varies between 90 degrees and 70 degrees relative to datum 12. In one embodiment, for example, axis 9 is oblique to datum surface 12 (shown in Fig. 16A). This is preferably achieved by impinging etchant at an acute angle to datum surface 12. In one embodiment there is achieved an asymmetrical undercut pattern that is characterized by an undercut face 165, of ellipsoid 166, that projects over cavity 20 a distance greater than the projection of the opposing face 164. In one embodiment, opposing face 164 does not overhang cavity 12. In one embodiment, the impingement of etchant at an angle produces a tilted saw-tooth or tiger-tooth structure 169 shown in FIG. 16B. Such structure allows relatively easy insertion into a bone channel 168 (e.g., when insertion is in a direction such that undercut 165 is not urged into bone B as in FIG. 16C), but strongly resists tensile force urging dislodgment of the implant (e.g., when removal is in a direction such that undercut 165 is urged into bone B as in FIG. 16D). In one embodiment, cavities 20 are aligned in series so that a cross-section of the textured surface has a regular pattern which may also be a repeating pattern (see, e.g., FIGs. 16C, 16D), 42A and 42B). FIGs. 42 A and 42B illustrate a comparison between the affects of directional and nondirectional impingement. FIG. 42B illustrates an embodiment of the invention where nondirectional impingement has been performed. In a preferred embodiment employing nondirectional impingement, the major axis 9 of complex ellipsoid 30 is substantially parallel with datum surface 12, and undercuts are present at the point 432 where the cross section of ellipsoid 30 intersects datum 12. In another embodiment illustrated in FIG. 42A, major axis 9 is oriented oblique to datum surface 12, there is an undercut 432 at the distal end 431 of cavity 20, and face 434 has no undercut at the proximate end 433 of cavity 20. In one embodiment, cavity 20, formed by directional etching, is defined by a concave surface 432 and a convex surface 434. Alternatively, opposing surfaces of cavity 20 may each have concave configurations (FIGs. 16C and 16D).
In one embodiment of implant 40 (illustrated in FIG. 41), unidirectional barbs 422 are produced in the surface that can be inserted into bone or tissue. The directional orientation of barbs 422 make it difficult to withdraw from the bone or tissue. In conditions where a directional or anisotropic geometry are not desired, simpler non-directional agitation such as a turbulently- flowing etchant bath, or ultrasonic cavitation can be employed.
FIG. 16 illustrates a prefeπed geometric relationship between surface 12 and ellipsoids 30a and 30b. The dimensions are typical and descriptive of a commonly achieved pattern, but are not restrictive. The skilled practitioner may vary these dimensions greatly depending on the desired outcome. In the embodiment illustrated, depth d of cavity 20 as measured from the datum 12a to bottom 4 is substantially 0.0210 inches. Major diameter a of ellipsoids 30a and 30b is substantially 0.0474. The distance b from datum 12 to the major axis 9 is substantially 0.0055 inches. Distance c along the major axis 9 between the perimeter of complex ellipsoid 30a to a point x projecting from the intersection of complex ellipsoid 30a with datum 12a is substantially 0.0012 inches. It follows, that distance e along major axis 9 between projection points x and y is substantially 0.0450 inches.
Returning to FIG. 13, there is illustrated prefeπed three dimensional texture 130. Texture 130 is embodied in an article 10 after the etching process described above. In this embodiment, while three dimensional pattern 130 may be of an iπegular pattern to the extent that the structural features of the pattern are unevenly distributed on a micro-level, this pattern is both repeatable across the device, and reproducible between devices.
The repeatable and reproducible nature of texture 130 is achievable through the employment of patterns (e.g., pattern 400 in FIG. 40) which may be seen by an observer. In one embodiment, the patterns are written into or through the maskant or etch resist layer by a laser as described herein. In another embodiment, the pattern is displayed as an image that can be seen by an observer on a computer monitor, printed output, or other such viewing device. In one embodiment, pattern 400 may be derived from an initial pattern having a regular series of elements that include one or more regular or iπegular geometric configurations such as circular dots, squares, prisms, parallelepipeds, trapezoids, triangles, hexagons, and other such geometric shapes that the practitioner deems suitable to generate the third-dimension development of the desired finished texture 130. In one embodiment, a pattern of repeated fractals or other pseudorandom network of elements are employed to generate the initial pattern. In practice when patterns are developed into three-dimensional patterns 130 by etching, they generally regularize rather than randomize. For example, an aπay of dots or other shapes will form boundaries as the suπounding material is removed by etching. When a connection density of portions of the etched surface peaks, sub-peaks, and intermediate peaks of approximately 58% is reached, a phenomenon known as "percolation threshold" forms, where networks of connections form.
FIGs. 17A, 17B, 17C, 17D, and 17E illustrate variations on the textured surface of the prefeπed embodiment. FIG. 17A illustrates textured surface 170 having a three-dimensional iπegular pattern that is characterized by multiple intersections of complex non-spherical ellipsoids that form peaks 5a and 5c. There is illustrated sub-peak 161 which is defined by a the intersection of at least two complex ellipsoids. A first complex ellipsoid defining sub- peak 161 further defines, at least a portion of cavity 162. A second complex ellipsoid defining at least a portion of cavity 163, intersects the first complex ellipsoid to define sub- peak 161. This configuration further illustrates a resulting texture where intersecting complex ellipsoids of varying angular projections are oriented with major axes at an offset angle to one another. For example, if the initial pattern used includes elongated elements, or sets of two or more dots, a first set oriented at one angle to a grid, and a second set oriented at another angle, then the etching and undercutting process will generate a series of ovoid shapes as viewed from the top, with long axes aligned to these grid lines. For example, one set of grid lines may be at an angle of 40 degrees to the other, resulting in a lozenge-shaped array.
Also illustrated in FIG. 17A is the effect of a scratch-fit where soft tissue shavings 160 have migrated into the voids 20 and are growing to fill the voids.
FIG. 17B illustrates textured surface 171 having a regular pattern. Each protrusion 2a in FIG. 17B has peak 5a coincident with outer surface 12 (not illustrated). There is furthermore, a geometry characterizing protrusion 2a that is defined by four (4) complex ellipsoids which have been uniformly oriented. Further characterizing this embodiment is a distance, f, between protrusions that is uniform among transverse and longitudinally adjoining protrusions. In this embodiment, distance f between protrusion 165a and 165b is substantially the same as the distance, g, between 165b and 165c. In alternative uniform embodiments, the distance between transversely adjacent protrusions may be different from the distance between longitudinally adjacent protrusions thus forming a "rectangular pattern" as opposed to a "square pattern". Any other geometrically uniform patterns are also within the scope of this invention. These include, as examples, ellipsoidal cavities substantially aπanged on a hexagonal, pentagonal, triangular, or other regular geometric lattice. FIG. 17C illustrates a uniform repeating pattern that combines a plurality of protmsion geometries including protrusions 166a defined by five (5) complex ellipsoids; protmsions 166b defined by four complex ellipsoids; and sub-peaks 166c defined by three complex ellipsoids 166c. In this embodiment, the horizontal orientation of adjoining protmsions varies in a substantially non-random pattern.
FIG. 17D illustrates protmsion 167b that is defined by a multiplicity of complex ellipsoids. Protmsion 167b has peak 167a that has been formed to project a scalloped surface 177. There is also shown intermediate peak 175 and sub-peak 176. In this embodiment, intermediate peak 175 has one face that is not undercut, or with undercut regions have been etched away in the process, and another face that is undercut.
FIG. 17E illustrates protmsion 168 that has been defined by a multiplicity of complex ellipsoids. In one embodiment, protmsion 168 extends for a predetermined length of the surface. In one embodiment, the predetermined length forms a rib. The top of rib 168 is preferably coincident with the datum surface 12. In other embodiments rib 168 has a sub peak or an intermediate peak. Alternatively, rib 168 has a combination of peaks, sub-peaks, and intermediate peaks. In this embodiment, each face 17 of protmsion 168 has an undercut surface. There is also illustrated protmsion 169 which is characterized by an intermediate peak 5b that was formed when the base material above the peak was broken-off, or where a top section became isolated or cut away by the interception of undercut regions. While some textured surface applications benefit from an undercut textured embodiments, the methods of the present invention can be used to create engineered articles. For example, certain embodiments are suited for creating an implant article having a mesh- and plate-surface (described below). In other embodiments, undercut textured surfaces are combined with mesh-and-plate surfaces. To make a mesh-and-plate surgical implant, there is provided a thin sheet 180 (FIG. 18) of tissue and bone compatible metal, such as titanium. A maskant layer 192 (FIG. 19) is applied to a first face 194 of the sheet 180 and a maskant layer 196 is applied to a second face 198 of the sheet 180. The maskant layers 192, 196 cover substantially the entirety of the first and second faces 194, 198, respectively. The maskant layers 192, 196 are resistant to chemical attack. It has been found that a photo-chemical resist, such as duPont Riston®, or Kodak Thin Film Resist®, serve as appropriate materials for the maskant layers 192, 196. The maskant layers 192, 196 are then in part ablated from selected portions of the metal faces 194, 198 (FIG. 20), as by mechanical tools, chemical milling, photo-chemical etching, or by laser eradication, to expose portions 202, 204, 206 of the respective metal faces 194, 198 in desired patterns, ready for etching.
Referring to FIG. 21, it will be seen that the exposed portions 204 of the first face 194 and the maskant layer 192 on the first face 194 are covered with a protective tape 210, leaving exposed only the region 202 where a central through-hole is desired for acceptance of a mounting screw (not shown). Similarly, the exposed portions 206 of the second face 198 and the maskant layer 196 on the second face 198 are covered with a protective tape 212. The tapes 210, 212 may be 3M Brand Type #1280 Platers Tape.
The through-hole region 202 is then subjected to etching, for example, as by spray or immersion, using an acid bath of a mixture of nitric and hydro fluoride acid. It is prefeπed, during the etching process, to periodically remove sheet 180 from the etching process and rinse, dry and bake the sheet to maintain the integrity of the maskant and allow for in-process inspections.
When the etchant reaching the exposed surface 202 has created a shallow crater 222 (FIG. 22), the protective tape 210 is removed (FIG. 23) and the etching of the crater 222 is resumed, and etching of the exposed portions 204, constituting the mesh portion of the implant, is undertaken. As etching proceeds, the exposed metal regions 222 and 204 are progressively removed by the etchant (FIG. 24). The etching continues until the removal of metal from the first face 194 and crater 222 has reached the predetermined extent desired (FIG. 25).
The second tape 212 is then removed, exposing the maskant layer 196 and exposed portions 206 on the second face 198, including an area 252 opposite the crater 222.
Etching of the through-hole area 252 in the sheet face 198 breaks through to the crater 222 to effect a counter-sunk through-hole 262 (FIG. 26) and second face openings 264 in communication with the newly etched first face 266.
The first and second maskant layers 192, 196 are then removed (FIG. 27), leaving an implant device having the mesh portion 272, a plate portion 274, and at least one through- hole 262 for receiving a mounting screw.
In FIG. 28 there is shown, for illustrative purposes, a dog-leg plate portion 274 having one or more through-holes 272 therein, the plate portion 274 being bounded by the mesh portion 272. In FIG. 29 there is shown a divided plate 292 having through-holes 262 therein, and bounded by the mesh portion 272.
Referring to FIG. 30, it will be seen that through-holes 262 may be provided in mesh portions 262, such through-holes preferably being suπounded by rim collars 302 comparable in thickness to a plate portion 274. The through-holes 262 preferably are countersunk to receive mounting screws. In an alternative embodiment, the maskant layers 192, 196 may be exposed to a movable laser beam which is moved in accordance with a path governed by a CAD data file, wherein the beam removes unwanted maskant. After the laser removes the maskant, the sheet 180 is exposed to heat and/or ultraviolet light to cure and harden the remaining maskant. The mesh portions 272 preferably are of a thickness of about .5 mm and are readily flexed to follow the curvature of a bone.
There is thus provided an improved method for making an article such as a mesh-and- plate surgical implant including both bendable perforated mesh portions and relatively rigid plate portions, wherein the bendable or comfortable perforated portions are integral with and kinematically related to the rigid plate portions. The improved method further provides through-holes for receiving mounting screws during implantation.
The performance of tissue implants may be enhanced by textured surface having undercut characteristics and/or mesh-and-plate characteristics. For example, where a textured surface is specified to promote osseointegration an undercut texture may be specified. Alternatively, where there is need to join the implant with a mechanical securement (e.g., a screw or bolt), the mesh-and-plate texture may be specified. It should be recognized that combining one or more of such textures on a single implant is a viable alternative within the scope of this invention.
FIG. 31 illustrates tissue implant 310, constmcted from a bio-compatible material such as metal, glass, plastic, and ceramic. In one prefeπed embodiment, the bio-compatible material is chemically pure (CP) titanium. Implant 310 is useful in any application in which a secure attachment to an object is desired and would be enhanced by using a textured surface such as discussed herein. Though dental applications and spinal applications have different mechanical objectives, the present invention is useful in both applications. Spinal devices, for example, preferably separate vertebrae in permanent alignment and transfer compressive forces between adjacent vertebrae. Bone ingrowth secures these devices into place, especially with the object of resisting forces that would tend to dislodge them. Dental devices, for example, are preferably screwed into a hole bored in the mandible, whereupon bone ingrowth locks them into place so that teeth or other appliances can be affixed to them. In this application, dental devices must resist tensile and compressive forces and transfer those forces to the bone sufficiently that the bone-to-appliance bond strength is not exceeded.
For example, implant 310 is useful for implantation and/or attachment to hard tissue such as bone in spinal and dental applications and soft tissue. In one embodiment, implant 310 may be adapted for use in a commercial spinal fusion device. Another embodiment of implant 310 may be adapted for use in dental applications, such as with a dental implant in tissue. In one embodiment, implant 310 is particularly well suited as a dental implant post onto which prosthetic teeth or other appliances may be attached.
Implant 310 has a longitudinal axis 311. Distal end 312 of implant 310 typically is inserted into tissue such as a bone (e.g., a jaw bone). In one embodiment, proximal end 314 may be adapted to receive a prosthesis such as an artificial tooth or other dental appliance.
As shown in FIG. 32, in one embodiment, implant 310 preferably has a wall 320 that is disposed about longitudinal axis 311. In one embodiment, wall 320 is radially disposed about axis 311, and wall 320 has an outer face 322, and an inner face 321. In one embodiment, one or both of outer face 322 and inner face 321 may be substantially parallel to axis 311. In a prefeπed embodiment, wall 320 is tapered such that distal end 312 of wall 320 has a smaller diameter about axis 311 than at proximal end 314 of wall 320. In one embodiment, wall 320 defines cavity 324.
It was known to use perforations in tissue implants to promote tissue inter-growth necessary to lock an implant to tissue, and to use perforations in tissue implants to vent heat and tissue during installation, as set forth in U.S. Patent No. 4,960,381, the entire contents of which are incorporated herein by reference. In an embodiment of the present invention, the textured surfaces described below are believed to satisfy one or both of those functions and implant 310 does not include any perforations in wall 320. In other embodiments, as shown in FIGS. 31, 35, 37A, 37B, and 37C, wall 320 includes one or more apertures 318 which permit the transmission of fluids (e.g., blood), tissue, and tissue fragments (e.g., bone fragments) into cavity 324 to promote, for example, tissue inter-growth (i.e., osseointegration) and/or a heat and/or tissue venting. Aperture 318 may be formed by any method including the methods described herein or other mechanical methods (e.g., drilling), chemical methods(e.g., chemical etching), and/or heat methods(e.g., laser). In one embodiment, apertures 318 are formed by chemical etching of one or both of outer surface 322. Apertures 318 may be more specifically formed by a chemical etching process applied to outer surface 322. In another embodiment, aperture 318 is formed by laser ablation and chemical etching process applied to both outer surface 322 and inner surface 321 such as the method used to create countersinks, mesh geometries and textures as described in U.S. Patent application Nos. 09/976,722 to Amrich et al., and 10/021,616 to Amrich; the entirety of each being incorporated herein by reference.
As shown in FIGs. 31 and 32, in prefeπed embodiments, there is at least one aperture 318 that is defined by aperture surface 323, extending between inner face 321 and outer surface 322. Aperture surface 323 may be of any geometry. In one embodiment, aperture surface 323 is substantially flat (e.g., is substantially in a two dimensional plane). In another embodiment, aperture surface 323 is curved such as concave, convex or a compound curve (e.g., a curve with both a concave and a convex component, and multiple concave or convex curves of varying radii and combinations thereof). In one embodiment, aperture surface 323 is disposed normal to axis 311. In another embodiment, aperture surface 323 is oblique to axis 311. Where aperture surface 323 is oblique to axis 311, that angle may be either acute or obtuse. Aperture surface 323 may also be disposed at varying angles to inner face 321 and outer surface 322. In a prefened embodiment, aperture surface 323 is at least partially a textured surface 351 as illustrated in FIG. 35 and as disclosed herein. In one embodiment, the textured surface 351 of aperture surface 323 has a texture that is characterized by undercut recesses such as is created from the methods described herein. Aperture 318 may be of varying sizes depending on their intended function. Aperture
318 can have any shape including curved (e.g., round aperture 371), angular (e.g., square aperture 372 and triangular (not shown)), complex geometric shapes (e.g., multi-curved aperture 373) and combinations thereof within any one aperture 318 or among different apertures 318 of the same implant 310 (as illustrated in FIG. 37A). In a prefeπed embodiment, aperture 318 has an oblong geometry with the maj or axis of aperture 318 longitudinally oriented and the minor axis transversely oriented to axis 311 as illustrated in FIG. 37C. Implant 310 may have one or more aperture 318. In one embodiment, where more than one aperture is included, apertures 318 are either angularly disposed to one another (e.g., less than 180° apart along face 321), longitudinally disposed (e.g., aligned along the longitudinal axis), disposed across from one another (e.g., at 180° relative to face 321), and in geometric combinations thereof. Apertures 318 may extend into the self-tapping region (discussed below) of implant 310.
In one embodiment, as shown in FIG. 36, one or both of outer wall 322 and inner wall 321 include one or more recesses 362 that do not extend through wall 320. Recesses 362 may be formed by any method as described with respect to aperture 318 and may include any attribute of size, shape, and/or configuration discussed with respect to aperture 318. Furthermore, any portion or all of recess 362 may include a texture surface as described.
As shown in FIGS. 31, 32, 33, 34, 35, 38 A, 38B, 39A, 39B, 39C, 38C, and 38D, in prefeπed embodiments, implant 310 may also include one or more protmsions 325 from outer face 322. In one embodiment, protmsions 325 may be one or more ribs 326. In one embodiment, ribs 326 may be helically disposed about longitudinal axis 311 to form threads 316 as illustrated in FIG. 31. An implant 310, having threads 316 may typically be installed by screwing implant 310 into tissue (e.g., bone). In one embodiment, thread 316 is continuous from a point approximately at distal end 312 to a point approximately at proximal end 314. In another embodiment, threads 316 may be discontinuous. Where thread 316 is discontinuous, the discontinuity may be at a location proximate to aperture 318 as illustrated in FIG. 31 , or the discontinuity may be located where there is no aperture as illustrated in
FIG. 38C.
In one embodiment, protmsions 325 are in the form of longitudinal ribs 382 (as illustrated in FIG. 38A and 33) longitudinally disposed on implant 310 such that ribs 382 n generally between proximal end 314 and distal end 312. In one embodiment ribs 382 mn generally parallel to axis 311. In another embodiment, angular ribs 383 may be disposed at an angle relative to axis 311, as illustrated in FIG. 38B. In another embodiment, transverse ribs 384 are disposed to form substantially concentric rings that are radially disposed about axis 311 as illustrated in FIG. 38D. Transverse ribs 384 can have any desired pitch angle. In one embodiment, transverse ribs 384 have a low pitch angle. In another embodiment, transverse ribs 384 have a pitch angle of substantially 0°. While longitudinal ribs 382, angular ribs 383, and transverse ribs 384 are shown to be substantially continuous from distal end 312 to proximal end 314, such ribs having discontinuities are also within the scope of the present invention. In one embodiment, ribs 326 may be in the form of discrete segments 335 protmding from wall 320. In one embodiment, discrete segments 335 are evenly distributed about axis 311. In one embodiment evenly spaced discrete segments 335 are of substantially uniform size. In another embodiment, discrete segments 335 are of varying sizes. In another embodiment, discrete segments are unevenly spaced. Ribs 326 may have any cross sectional geometry including v-shaped, keystone shaped (e.g., rib 343), curved (e.g., rib 344), trapezoidal with an exterior short face (e.g., rib 348), trapezoidal with an exterior long face (e.g., rib 347), undercut (e.g., rib 345), hourglass (e.g., rib 349) and square (e.g., rib 346), as shown in FIG. 34. In one embodiment, ribs 326 on implant 310 are in the form of longitudinal ribs T32 having one or more of several geometries as shown in Figs 32, 33, 34.
It may be necessary, in some procedures, to drill at least one pilot hole or successively larger pilot holes to accommodate implant 310 prior to screwing implant 310 into the tissue. In another embodiment, it may be desirable to drill a large-enough hole where implant 310 can be tapped into place with a mallet. Typically, for implant 310, those embodiments having non-helical ribs are suited for tapping in place while those embodiments including threaded ribs are suited for screwing in place.
In a prefeπed embodiment, implant 310 may be configured to include a self-tapping thread 317 that is helically disposed about longitudinal axis 311 , as shown in FIG. 31. Where self-tapping threads 317 are employed, installation may be accomplished with no pilot hole or with smaller diameter pilot holes than if the self-tapping thread 317 was not included. Self- tapping threads 317 of a prefeπed embodiment, has a thinner web thickness and more root dimension than crest spacing. The ribs may therefore, appear to be more widely spaced apart. Where self-tapping threads are used, sufficient anchoring can be achieved while reducing the amount of material (e.g., tissue) that is cut or displaced. The tapping force requirement to install a device with the self-tapping features is lower than is necessary for non self-tapping threads.
In one embodiment, threads T13 on implant 310 include one or more portions that are non self-tapping threads. For example, in one embodiment, only a distal portion of the threaded area of implant 310 is self-tapping. As shown in a prefeπed embodiment of FIG. 32, protmsions according to the present invention, have a height, h, suitable to restrict removal of implant 310, for example, by the application of axial, longitudinal, and/or radial force.
In one embodiment, outer face 322 and ribs 326 are textured over substantially their entire surface. In another embodiment, outer surface 322 and ribs 326 have textured portions and portions that are relatively smooth (e.g., not textured). More particularly, where a portion of ribs 326 are relatively smooth, that portion may be the crests 392 of ribs 326 as shown in FIG. 39A. In another embodiment, as illustrated in FIG. 39A, outer face 322 is at least partially textured, and ribs 326 are non-textured. Leaving crests 392 without texture is believed to facilitate the installation of implant 310, for example, by avoiding excessive fragmentation to tissue (e.g., bone) suπounding the distal end of implant 310. In a prefeπed embodiment, outer surface 322 is textured and ribs 326 are not textured. In other embodiments regions of texturing and non-texturing may be used on inner face 321, outer surface 322, aperture surface 323, and ribs 326. In one embodiment, inner face 321 is textured as illustrated in FIG. 39B. In another embodiment, inner face 321 is textured and there are alternating regions of outer surface 322 that are textured as illustrated in FIG. 39C.
Known devices, incorporate an anti-rotation fixture (which may include a hollow cross-drilled stmcture) that locks the screw device into permanent immobility when bone ingrows the fixtures Such a stmcture may further serve as a vent during installation. In one embodiment of the present invention, the locking mechanism is integral to the surface of a portion of the threads thus eliminating the need for an additional anti-rotation fixture. In Niznick (U.S. Pat. No. 5,571,017), for example, an anti-rotation fixture characterizes approximately one-third of the device.
In one embodiment, a textured surface may be described as having a higher fractal dimension than a non- textured surface. Depending on the nature of the implant, the fractal dimension may be specified based upon the nature of the implant. For example, where the scratch- fit properties of the implant (e.g., as described above) is of primary importance, a greater fractal dimension may be specified to improve the tissue harvest during implantation. Alternatively, where strength of the bond created by the thread alone is of primary importance, a lower fractal dimension may be specified to limit the dismption of host tissue during implantation. Furthermore, single implant may have regions of varying fractal dimensions that may be dictated by the function of each region on the implant. In a prefeπed embodiment, a distal region of the implant, that anchors the implant in a tissue, has a lower fractal dimension than a more proximal region that is designed with a preference toward the promotion of tissue growth over short term strength. In another embodiment, regions of higher and lower fractal dimension may alternate along the longitudinal axis 311.
Where a textured component on implant 310 is designed to promote a scratch-fit with tissue that accepts implant 310, the scratch- fit is believed to promote faster healing time by, for example, auto-grafting the patient's bone into the interstices of the surface geometry and causing less compressive trauma to the bone. In one embodiment, the interference fit of the appliance 310 into the prepared site causes the patient's bone B to be shaved by the sharp edges of the surface texture. Since the bone matter is "donated" by the patient, the resulting autograft allows faster healing than is possible with bone matter provided by bone bank donors. The bone matter in one embodiment, originates from the patient and does not need to be denatured, or otherwise have its vitality compromised. In a further embodiment, the bone matter is instantly used as a growth lattice with no local immune reactions. The bone matter may thus be regarded as "alive". Even where a textured surface does not scratch the tissue, it provides a bedding upon which tissue fragments may accumulate and seed. In a prefeπed embodiment, the elliptical cavities of the textured surface becomes filled with the shavings from the patient's bone without compromising the vitality of shavings and thus not requiring a denaturing step. This bone matter is, therefore, instantly available for growth lattice without local immune reactions. In addition to promoting faster healing times, the higher fractal dimension of the textured surface (relative to a non-textured surface) is believed to ensure a higher shear strength of the bond between the implant and the host tissue. During installation of a prefeπed embodiment, where ribs 393 are not textured and surface 322 is textured, ribs 393 are believed to initially retain the implant. Where implant 310 is tapered about axis 311, once implant 310 is seated (e.g., pressed or driven to its intended installation depth, or to the depth of the preliminary reaming or drilling), the taper promotes harvesting of bone into the textured surface. In one embodiment, as the device is rotated (e.g., screwed into the host bone), the widening shape generates radial forces that act as a progressively tightening fit.
One may evaluate the benefits gained from implementing these prefeπed embodiments by observing the coπelation between the fractal information dimension and the "pin pushout strength" of a textured body. "Pin pushout strength" refers to a test where candidate textures are applied to small metal dowels. Holes are bored into femur bone in a test subject (canine), and the test sample dowels are pressed into the bores, using a fixture to assure straight and uniform placement. After sufficient time is allowed for healing and bone growth, the bone is removed by pressing the dowel with a pin. The amount of force required to press out the dowel with the pin is measured and recorded by an Instron® tester or similar apparatus. This measures the shear strength of the bone-to-implant bond. Of the samples tested, those embodying the present invention did not fail at the bond line, but rather at some distance outward from the bond line into the vital bone. This result demonstrates that the strength of the implant-to-bone bond was greater than the strength of the host bone itself. In general terms, the greater the fractal information dimension the greater the pin pushout strength which is a quantifiable measurement of bond between a prosthetic body and the tissue to which it is attached.
Tests were performed to compare some embodiments of the present textured surfaces with those of known textured surfaces. The tests include quantifying the degree of roughness attributable to these competing embodiments and comparing that roughness to the effectiveness of an implant bonded with the embodied textured surfaces. The degree of roughness was quantified using the fractal analysis program BENOIT v.1.3, (developed by Trusoft International, Inc. of St. Petersburg, Florida).
In the study of natural biological growth and many other applications of fractal analysis, it is often appropriate to employ a variation of the "Box Dimension Method" where not only the number of boxes penetrated by the pattern are counted, but where the degree of penetration, or extent of box contents, is weighted in the calculation. This modified method is called the "Information Dimension Method." Both the Box Dimension Method and the Information Dimension Method are described in the literature accompanying the BENOIT software, which is incorporated by reference in its entirety herein.
The simplest method of measuring the fractal dimension of a surface is to photograph a cross section of the prepared surface, and render the outline as a simple white line on a black background in an image stored as a bitmap (BMP) file for processing by the program. If such a line is superimposed on a grid, and the number of boxes penetrated by the line is counted, and repeated at successively smaller box sizes, then plotted in log-log axes, a scale- independent number is reached.
As described in Benoit's software, the box dimension is defined as the exponent Db in the relationship:
Eq. (la) N(d)~ 1/d ΛDb where N(d) is the number of boxes of linear size, d, necessary to cover a data set of points distributed in a two-dimensional plane. The basis of this method is that, for objects that are Euclidean, Eq. (la) defines their dimension. One needs a number of boxes proportional to 1/d to cover a set of points lying on a smooth line, proportional to l/dΛ2 to cover a set of points evenly distributed on a plane, and so on.
This dimension is sometime called grid dimension because for mathematical convenience the boxes are usually part of a grid. One could define a box dimension where boxes are placed at any position and orientation, to minimize the number of boxes needed to cover the set. It is obviously a very difficult computational problem to find, among all the possible ways to cover the set with boxes of size d, the configuration that minimizes N(d). Also, if the overestimation of N(d) in a grid dimension is not a function of scale (i.e., we overestimate N(d) by, say, 5% at all box sizes d), which is a plausible conjecture if the set is self-similar, then using boxes in a grid or minimizing N(d) by letting the boxes take any position is bound to give the same result. This is because a power law such as Eq. (la) is such that the exponent does not vary if we multiply N(d) or d by any constant.
In practice, to measure Db, one counts the number of boxes of linear size d necessary to cover the set for a range of values of d; and plot the logarithm of N(d) on the vertical axis versus the logarithm of d on the horizontal axis. If the set is indeed fractal, according to BENOIT, this plot will follow a straight line with a negative slope that equals minus Db. To obtain points that are evenly spaced in log-log space, it is best to choose box sizes d that follow a geometric progression (e.g., d = 1, 2, 4, 8,...), rather than use an arithmetic progression (e.g., d = 1, 2, 3, 4,...).
A choice to be made in this procedure is the range of values of d. Trivial results are expected for very small and very large values of d. A conservative choice may be to use as the smallest d ten times the smallest distance between points in the set, and as the largest d the maximum distance between points in the set divided by ten. Alternatively, one may exceed these limits and discard the extremes of the log-log plot where the slope tends to zero.
In theory, for each box size, the grid should be overlaid in such a way that the minimum number of boxes is occupied. This is accomplished in Benoit by rotating the grid for each box size through 90 degrees and plotting the minimum value of N(d). Benoit permits the user to select the angular increments of rotation.
In the study of natural biological growth and many other applications of fractal analysis, it is often more appropriate to employ a variation of the Box Dimension method where not only the number of boxes penetrated by the pattern are counted, but where the degree of penetration, or extent of box contents is weighted in the calculation. This is the Information Dimension Method.
The Information Dimension is often encountered in physics literature, and is generally different from the box dimension. In the definition of box dimension, a box is counted as occupied and enters the calculation of N(d) regardless of whether it contains one point or a relatively large number of points. The information dimension effectively assign weights to the boxes in such a way that boxes containing a greater number of points count more than boxes with less points.
The information entropy 1(d) for a set of N(d) boxes of linear size d is defined as
N(d)
Eq. (lb) /(< = - ∑ ™, log( ,) where mas:
Eq.(2) !», = *.
where M, is the number of points in the i-th box and m is the total number of points in the set.
Consider a set of points evenly distributed on the two-dimensional plane. In this case, we will have
Eq. (3) N(d) * -k-
m. d2
so that Eq. (2) can we written as:
1
Eq. (4) : 1(d) * -N(d)[d2\ %2) » -— [2d ιog(d)] = -21og(d)
1(d) « -log(d) For a set of points composing a smooth line we would find:
Therefore, we can define the information dimension D, as in
Eq. (5) I(d) * Dtlog(d)
In practice, to measure D, one covers the set with boxes of linear size d keeping track of the mass m, in each box, and calculates the information entropy 1(d) from the summation in [Eq. (lb)]. If the set is fractal, a plot of 1(d) versus the logarithm of d will follow a straight line with a negative slope equal to -D,. It was noted above that the information dimension differs from the box dimension in that it weighs more heavily boxes containing more points. To see this, let us write the number of occupied boxes N(d) and the information entropy 1(d), in terms of the masses m, contained in each box:
Eq. (6) N(d) = ∑ m; ;I(d) = -∑ml\og(ml)
The first expression in Eq. (6) is a somewhat elaborate way to write N(d), but it shows that each box counts for one, if m, > 0. The second expression is taken directly from the definition of the information entropy Eq. (lb). The number of occupied boxes, N(d), and the information entropy 1(d) enter on different ways into the calculation of the respective dimensions, it is clear from [Eq. (6)] that:
Eq.(7) DK ≤ D.
The condition of equality between the dimensions [Eq. (7)] is realized only if the data set is uniformly distributed on a plane.
The following table illustrates the relationship between the Information Dimension of certain textural products and the Pin Pushout strength for selected products. Also illustrated in the following table is the standard deviation of the Information Dimension as calculated by the Benoit software. Higher standard deviations number are illustrative of a more "random", less ordered surface texture.
TABLE 1 :
Figure imgf000049_0001
Figure imgf000050_0001
In any of the above embodiments, one or more of the elements described may be included in implant 310. For example, textured portion 351 has any desired texture depending on the particular use of implant 310. For example, textured portions 351 may include patterns formed from the methods described herein. Textured portions may also include random patterns as described in U.S. Patent No. 5,258,098, U.S. Patent No. 5,507,815, U.S. Patent No. 5,922,029, and U.S. Patent No. 6,193, 762 each issued to Wagner et al., the entire contents of which are hereby incorporated by reference. The textures may also include the patterns described in U.S. Patent No. 5,975,903 issued to Shoher et al., U.S. Patent No. 6,095,817 issued to Wagner et al., U.S. Patent No. 6,217,333 Bl issued to Ercoli, U.S. Patent No. 5,571,017 issued to Niznick, U.S. Patent No. 5,639,237 issued to Fontenot, and U.S. Patent No. 4,960,381 issued to Niznick the entire contents of which are hereby incorporated by reference.
Referring to FIGS. 43 and 44, it will be seen that a typical hip-replacement assembly, or prosthesis, includes a femoral stem 4302 having a neck portion 4304 to which there is fixed a ball-like head 4306. The head is received in a lining 4308, which is disposed in an acetabular cup 4510. The acetabular cup 4510 is provided with a datum surface 12, which is adapted for engagement with a bone. The datum surface 12 is provided with a multiplicity of undercut micro recesses 20, described hereinbelow. The micro recesses 20 may be provided in accordance with methods set forth above.
In one embodiment, there is provided a complex, at least in part interconnecting pattem, or similar 3-dimensional surface, which enhances the attachment of bone to the surface of the implant.
Briefly, the undercut micro recesses 20 are produced as follows:
There first is provided the acetabular cup 4510 of one of titanium, zirconium, stainless steel and alloys thereof, tantalum, refractory metals, metal carbides, cobalt-chromium, and alloys thereof, and ceramics, plastics and glass, and composites of metals, ceramics, plastics, and glass, or a material similar thereto. The cup 4510 is provided with the datum surface 12 (FIG. 45) in which it is desired to provide a multiplicity of undercut recesses 20.
As shown in FIG. 46, a layer 14 of maskant material is deposited on substantially the entirety of the datum surface 12. The maskant is a suitable acrylic, epoxy, or polyester resist, or the like, or any other maskant such as identified herein. The layer 14 may be applied by dipping, spray-coating, or electrostatic-depositing to produce a layer thickness of about 0.001-0.010 inch.
Selected areas 16 of the layer 14 (FIG. 47) are then removed to expose portions 18 of the datum surface 12. The use of computer-directed direct laser ablation to generate programmed patterns in the maskant layer 14 allows the application of such patterns to the compound curves of the acetabular cup 4510.
To generate a selected image, or aπay of recesses, or a fractal pattern, in a laser receptive maskant, the use of a computer-directed laser to directly ablate the maskant or etch resist layer in selected loci is prefeπed. The pattern produced by laser ablation is predictable and can be accurately duplicated and repeated from implant to implant.
The exposed portions 18 of the surface 12 are etched, preferably using a spray etcher at 100°F spray temperature and 10 lbs/in2 spray pressure, in a Nitric and Hydrofluoric Acid solution for about 20 minutes. Sufficient "fresh" etchant is continuously impinged upon the etch surfaces 18 to encourage lateral, as well as vertical, etching. It will be understood that alternative etching processes, such as immersing ultrasonics and electrolytic etching, can produce similar results. The etching produces recesses 20 that are undercut, as shown in FIG. 48, and that are, in part, interconnected, as at 22. The metal is etched in such a manner as to deliberately cause undercutting of the pattern, and to permit connection, joining, or "breakthrough" of some of the recesses 20 so as to produce a sharply defined complex network stmcture, including an interconnecting pattern in which the size of most of the recesses 20 is smaller at the surface 12 than at a plane some distance below the surface 12 of the article 4510. The recesses 20 may, in at least some instances, interconnect at and near the surface 12, as at 22 in FIG. 48, to provide enlarged surface recesses 20a (FIG. 49). The etching of the metal surface 12 is thus carried out in one step, wherein non- spherical ovoid-shaped recesses 20 are created, featuring desired sizes and depths that are repeatable from implant to implant.
The remaining resist may be removed (FIG. 49) by immersing the body surface 12 in an ND/Phase 23 Stripper bath at about 180°F for about 10 minutes. Alternatively, the maskant layer may be removed by solvation or emulsification. If desired, the article 4510 may be lightly post-etched.
In implantation, the implant surface 12 is pressed against the bone B (FIGS. 50 and 51) such that sharp edges 24 of the recesses 20 effect the "scratch fit" with the bone B, which involves shaving off, or milling, particulate segments b of the bone B, which segments b enter the ovoid recesses 20 (FIG. 46) wherein, in due course, the harvested bone segments b stimulate ingrowth of the bone B (FIGS. 52-54) to securely lock the implant to the bone B (FIG. 54).
The milling of the host bone B further serves to ream the bone B to the precise size and configuration of the cup 4510, ensuring the best possible fit. The scratch- fit securely adjoins the implant article 4510 to the bone B, to prevent or minimize micro motion between the body 4510 and bone B. The presence of such motion would discourage the ingrowth of bone into the implant and thereby discourage the long-term interconnection of the implant and bone. Further, the scratch-fit application of the implant to the bone harvests bone particulate matter that falls into the surface recesses and is retained by the recesses to encourage and stimulate ingrowth of the bone into the recesses. Inasmuch as the recesses are of an ovoid configuration, they provide a greater subsurface fractal area than spherically shaped recesses, and thereby a greater area for engagement of the bone material and the implant. Thus, the cup itself can be used as a reaming tool, effecting a perfect fit to the host bone and shortening healing time. Further, in the process of self-fitting, there are milled, or harvested, fine bone particulates, or pulp, from the patients' own body. The resulting material is forced into the recesses to serve as a nucleation host for a spontaneous homograft completed by the attraction and growth of the patient's osteoblasts, providing a strong bond and longer installed lifetime.
It will be understood that many additional changes in the details, materials, steps and aπangement of parts, which have been herein described and illustrated in order to explain the nature of the invention, may be made by those skilled in the art within the principles and scope of the invention. For example, while the recesses are shown with a central axis generally normal to the curved datum surface, it will be apparent that the recess axes can be "tilted" to provide asymmetrical undercutting. By etching out the recesses at an angle, a tilted saw-toothed stmcture (not shown) can be realized. Such a stmcture allows relatively easy insertion into a bone cavity, but strongly resists tensile force urging dislodgment of the cup. Although the foregoing description is directed to the prefeπed embodiments of the invention, it is noted that many additional changes, variations and modifications in the details, materials, steps and aπangement of parts, which have been herein described and illustrated in order to explain the nature of the invention, will be apparent to those skilled in the art, and may be made without departing from the spirit or scope of the invention.
All references refened to herein are hereby incoφorated by reference in their entirety.

Claims

We Claim:
1. A textured surface comprising: a base material having a cavity at least partially defined by at least one ellipsoid; and
an undercut projecting over the cavity.
2. The textured surface of claim 1 wherein: the cavity is at least partially defined by more than one ellipsoid, the undercut is at least partially defined by a first elliposid having a major axis, the cavity has a bottom surface at least partially defined by a second ellipsoid having a major axis substantially coincident with the major axis of the second ellipsoid.
3. The textured surface of claim 2 wherein the first ellipsoid has a wider angular projection than the second ellipsoid.
4. The textured surface of claim 1 wherein the ratio of cavity width to cavity depth is at least about 1.
5. The textured surface of claim 1 further comprising a protmsion extending from the bottom surface, the protmsion being defined by at least two of the ellipsoids.
6. The textured surface of claim 5 further comprising an outer surface wherein the protmsion comprises a peak coincident with the outer surface.
7. The textured surface of claim 5 wherein the protmsion further comprises a sub-peak defined by at least two overlapping ellipsoids.
8. The textured surface of claim 5 wherein the protmsion further comprises an intermediate peak located proximate the shortest distance between the at least two ellipsoids.
9. The textured surface of claim 5 wherein the protmsion is defined by at least two non- overlapping ellipsoids.
10. The textured surface of claim 6 wherein the peak overhangs a least a portion of the cavity.
11. The textured surface of claim 1 the base further comprising: an outer surface including a datum; a first protmsion having a peak coincident with a datum; a second protmsion having a sub-peak defined by at least two overlapping ellipsoids;
and a third protmsion having an intermediate peak located between at least two spaced- apart ellipsoids.
12. The textured surface of claim 1 further comprising a plurality of protmsions extending from the bottom surface, each protmsion being defined by one or more ellipsoids.
13. The textured surface of claim 12 wherein the plurality of protmsions are spaced in a regular pattern.
14. The textured surface of claim 13 wherein the regular pattern is substantially a grid.
15. The textured surface of claim 13 wherein the regular pattern is substantially a fractal pattern.
16. The textured surface of claim 12 wherein the plurality of protmsions are spaced in a repeating iπegular pattern.
17. The textured surface of claim 16 wherein the repeating iπegular pattern is substantially a fractal pattern.
18. The textured surface of claim 1 further comprising a protmsion defined by at least four ellipses.
19. The textured surface of claim 1 wherein the base material is selected from the group consisting of metal, ceramic, glass, and composites thereof.
20. A textured surface comprising: a multiplicity of cavities aπanged in a substantially reproducible pattern the cavities comprising a bottom surface geometry at least partially defined by a first ellipsoid, and an undercut overhanging a cavity and at least partially defined by a second ellipsoid having a major axis coincident with the first ellipsoid, the second ellipsoid having a wider angular projection than the first ellipsoid.
21. In a prosthetic device having a tissue engaging surface, a pattern comprising: a cavity recessed from the tissue engaging surface; a plurality of curved concave surfaces at least partially defined by a complex ellipsoid, the plurality of concave surfaces at least partially defining the bottom of the cavity; a plurality of projections extending from the bottom of the cavity, the projections having at least one undercut surface at least partially defined by a complex ellipsoid geometry, a portion of the tissue engaging surface laterally extending beyond the cavity to further define the undercut surface.
22. The prosthetic device of claim 21 wherein the complex ellipsoid is a non-sherical complex ellipsoid.
23. The prosthetic device of claim 21 wherein the plurality of curved concave surfaces are serially aligned to form a repeating pattern.
24. The prosthetic device of claim 23 wherein the repeating pattern is a saw-tooth pattern.
25. A prosthetic securement comprising: a base material having a reticulate surface with a multiplicity of undercut interconnected recesses at least partially defined by a complex ellipsoid; and a soft-tissue, scratch- fit to the textured surface in promotion of tissue growth within the interconnected recesses.
26. A tissue implant comprising: an outer surface having a datum surface and defining a cavity having a geometry characterized by at least one complex ellipsoid, and an undercut face projecting over a portion of the cavity.
27. The tissue implant of claim 26 having a rib outwardly protruding from the datum surface.
28 The tissue implant of claim 27 wherein the rib is a thread.
29. The tissue implant of claim 28 wherein the thread is a self-taping thread.
30. The tissue implant of claim 28 comprising a first end and a second end, the thread extending from proximate the first end to proximate the second end.
31. The tissue implant of claim 28 wherein the thread is continuous.
32. The tissue implant of claim 28 wherein the thread is segmented.
33. The tissue implant of claim 27 wherein the rib comprises a cross sectional geometry taken from the group consisting of v-shaped, keystone, curved, trapezoidal, undercut, hourglass, and square.
34. The tissue implant of claim 27 wherein the rib comprises a rib surface that is substantially smooth.
35. The tissue implant of claim 26 further comprising a longitudinal axis, and a plurality of ribs outwardly projecting from the outer surface, the ribs being radially disposed about the longitudinal axis.
36. The tissue implant of claim 35 wherein the ribs are substantially parallel to each other.
37. The tissue implant of claim 27 wherein the ribs are longitudinally disposed on the implant.
38. The tissue implant of claim 35 wherein the ribs are disposed on the implant oblique to
the longitudinal axis.
39. The tissue implant of claim 27 further comprising: a longitudinal axis, a wall, disposed about the longitudinal axis, characterized by an inner surface and the outer surface, and an aperture extending from the inner surface to the outer surface.
40. A tissue implant comprising: a base disposed about a longitudinal axis; a rib protmding outwardly from the base; and a textured surface on the base having a datum, a plurality of interconnected recesses abutting the datum, and an undercut face projecting over a portion of the recesses.
41. The tissue implant of claim 40 wherein the interconnected recesses further comprise a geometry defined by a non-spherical ovoid.
42. The tissue implant of claim 41 wherein the non-spherical ovoid is a complex ellipsoid.
43. The tissue implant of claim 40 wherein base further comprises a wall, disposed about the longitudinal axis, having a first outer surface and the rib further comprises a second outer surface contiguous with the first outer surface, the textured surface being at least a portion of the first outer surface, and at least a portion of the second outer surface being substantially smooth.
44. The tissue implant of claim 40 wherein the wall further comprises an aperture defined by an inner surface.
45. The tissue implant of claim 44 wherein the textured surface is at least a portion of the inner surface.
46. The tissue implant of claim 40 wherein the interconnected recesses have a geometry at least partially defined by a complex ellipsoid having a major axis oblique to the datum.
47. The tissue implant of claim 40 wherein the interconnected recesses have a geometry at least partially defined by a complex ellipsoid having a major axis oblique to the longitudinal axis.
48. The tissue implant of claim 40 wherein the interconnected recesses have a geometry at least partially defined by a complex ellipsoid having a major axis oblique to the datum.
49. The tissue implant of claim 40 wherein the interconnected recesses have a geometry at least partially defined by a complex ellipsoid having a major axis oblique to the longitudinal axis and to the datum.
50. A method for relieving strain from a titanium surface comprising: applying a maskant to the titanium surface; ablating at least a portion of the maskant to expose the surface; etching the exposed surface to relieve strain from the titanium.
51. The method of claim 50 wherein the etching further comprises forming interconnected recesses that are at least partially defined by non-spherical complex ellipsoids.
52. The method of claim 51 wherein the ablating further comprises laser ablating.
53. The method of claim 51 wherein the laser ablating increasing a localized strain proximate the portion of the ablated maskant.
54. A strain relieved implant comprising: a base material having a datum surface; a surface skin beneath the datum; and a plurality of interconnected recesses abutting the datum wherein the skin is substantially from strain.
5. A surface including a stmcture comprising: a plateau; a cavity beneath the plateau, and a concave face depending from the plateau and extending over the cavity.
PCT/US2002/039743 2001-12-12 2002-12-12 Textured surface having undercut micro recesses in a surface WO2003053669A1 (en)

Priority Applications (5)

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EP02792362A EP1463630A1 (en) 2001-12-12 2002-12-12 Textured surface having undercut micro recesses in a surface
JP2003554419A JP2005512702A (en) 2001-12-12 2002-12-12 Textured surface with undercut fine depressions on the surface
AU2002357821A AU2002357821A1 (en) 2001-12-12 2002-12-12 Textured surface having undercut micro recesses in a surface
CA002470068A CA2470068A1 (en) 2001-12-12 2002-12-12 Textured surface having undercut micro recesses in a surface
MXPA04005702A MXPA04005702A (en) 2001-12-12 2002-12-12 Textured surface having undercut micro recesses in a surface.

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US34028601P 2001-12-12 2001-12-12
US60/340,286 2001-12-12
US35645902P 2002-02-11 2002-02-11
US60/356,459 2002-02-11
US38803302P 2002-06-12 2002-06-12
US60/388,033 2002-06-12
US39195702P 2002-06-25 2002-06-25
US60/391,957 2002-06-25
US10/202,575 US7018418B2 (en) 2001-01-25 2002-07-24 Textured surface having undercut micro recesses in a surface
US10/202,575 2002-07-24

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JP (1) JP2005512702A (en)
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009000774A1 (en) * 2007-06-22 2008-12-31 Societa' Azionaria Materiale Ospedaliero - S.A.M.O. S.P.A. Method for producing surfaces for metal articles
EP2286767A1 (en) * 2009-08-21 2011-02-23 Jossi Holding AG Method for producing a structured surface on a workpiece from a metallic material and implant with such a surface

Families Citing this family (148)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5609635A (en) * 1988-06-28 1997-03-11 Michelson; Gary K. Lordotic interbody spinal fusion implants
US6695848B2 (en) * 1994-09-02 2004-02-24 Hudson Surgical Design, Inc. Methods for femoral and tibial resection
US8603095B2 (en) 1994-09-02 2013-12-10 Puget Bio Ventures LLC Apparatuses for femoral and tibial resection
US8062377B2 (en) 2001-03-05 2011-11-22 Hudson Surgical Design, Inc. Methods and apparatus for knee arthroplasty
EP1434607A1 (en) * 2001-10-11 2004-07-07 Straumann Holding AG Osteophilic implants
EP1575456B1 (en) 2002-12-20 2011-02-09 Smith & Nephew, Inc. High performance knee prostheses
US8251700B2 (en) * 2003-05-16 2012-08-28 Biomet 3I, Llc Surface treatment process for implants made of titanium alloy
GB0316934D0 (en) * 2003-07-19 2003-08-27 Xaar Technology Ltd Method of manufacturing a component for droplet deposition apparatus
JP2006528515A (en) * 2003-07-24 2006-12-21 テコメット・インコーポレーテッド Spongy structure
US7857814B2 (en) * 2004-01-14 2010-12-28 Hudson Surgical Design, Inc. Methods and apparatus for minimally invasive arthroplasty
US7815645B2 (en) * 2004-01-14 2010-10-19 Hudson Surgical Design, Inc. Methods and apparatus for pinplasty bone resection
US9814539B2 (en) 2004-01-14 2017-11-14 Puget Bioventures Llc Methods and apparatus for conformable prosthetic implants
US8021368B2 (en) * 2004-01-14 2011-09-20 Hudson Surgical Design, Inc. Methods and apparatus for improved cutting tools for resection
US20060030854A1 (en) 2004-02-02 2006-02-09 Haines Timothy G Methods and apparatus for wireplasty bone resection
US8114083B2 (en) 2004-01-14 2012-02-14 Hudson Surgical Design, Inc. Methods and apparatus for improved drilling and milling tools for resection
US7337528B2 (en) * 2004-12-23 2008-03-04 Motorola, Inc. Textured dielectric patch antenna fabrication method
US8323348B2 (en) * 2005-02-22 2012-12-04 Taiyen Biotech Co., Ltd. Bone implants
US7931681B2 (en) * 2005-04-14 2011-04-26 Warsaw Orthopedic, Inc. Anti-backout mechanism for an implant fastener
US20060247789A1 (en) * 2005-04-29 2006-11-02 Sdgi Holdings, Inc. Method and device for stabilization of prosthetic devices
US7824433B2 (en) * 2005-05-03 2010-11-02 Williams Lytton A Bone anchored surgical mesh
US8758442B2 (en) 2005-05-06 2014-06-24 Titan Spine, Llc Composite implants having integration surfaces composed of a regular repeating pattern
US8992622B2 (en) 2005-05-06 2015-03-31 Titan Spine, Llc Interbody spinal implant having a roughened surface topography
US8480749B2 (en) 2005-05-06 2013-07-09 Titan Spine, Llc Friction fit and vertebral endplate-preserving spinal implant
US8403991B2 (en) 2005-05-06 2013-03-26 Titan Spine Llc Implant with critical ratio of load bearing surface area to central opening area
US9168147B2 (en) 2005-05-06 2015-10-27 Titan Spine, Llc Self-deploying locking screw retention device
US8562685B2 (en) 2005-05-06 2013-10-22 Titan Spine, Llc Spinal implant and integration plate for optimizing vertebral endplate contact load-bearing edges
US8591590B2 (en) 2005-05-06 2013-11-26 Titan Spine, Llc Spinal implant having a transverse aperture
US8262737B2 (en) 2005-05-06 2012-09-11 Titan Spine, Llc Composite interbody spinal implant having openings of predetermined size and shape
US8585767B2 (en) 2005-05-06 2013-11-19 Titan Spine, Llc Endplate-preserving spinal implant with an integration plate having durable connectors
US8585766B2 (en) 2005-05-06 2013-11-19 Titan Spine, Llc Endplate-preserving spinal implant with an integration plate having durable connectors
US8551176B2 (en) 2005-05-06 2013-10-08 Titan Spine, Llc Spinal implant having a passage for enhancing contact between bone graft material and cortical endplate bone
US8814939B2 (en) 2005-05-06 2014-08-26 Titan Spine, Llc Implants having three distinct surfaces
US8562684B2 (en) 2005-05-06 2013-10-22 Titan Spine, Llc Endplate-preserving spinal implant with an integration plate having a roughened surface topography
US20120312779A1 (en) 2005-05-06 2012-12-13 Titian Spine, LLC Methods for manufacturing implants having integration surfaces
US8617248B2 (en) 2005-05-06 2013-12-31 Titan Spine, Llc Spinal implant having variable ratios of the integration surface area to the axial passage area
US9125756B2 (en) 2005-05-06 2015-09-08 Titan Spine, Llc Processes for producing regular repeating patterns on surfaces of interbody devices
US8545568B2 (en) 2005-05-06 2013-10-01 Titan Spine, Llc Method of using instruments and interbody spinal implants to enhance distraction
US11096796B2 (en) 2005-05-06 2021-08-24 Titan Spine, Llc Interbody spinal implant having a roughened surface topography on one or more internal surfaces
US8585765B2 (en) 2005-05-06 2013-11-19 Titan Spine, Llc Endplate-preserving spinal implant having a raised expulsion-resistant edge
US8435302B2 (en) 2005-05-06 2013-05-07 Titan Spine, Llc Instruments and interbody spinal implants enhancing disc space distraction
US8758443B2 (en) 2005-05-06 2014-06-24 Titan Spine, Llc Implants with integration surfaces having regular repeating surface patterns
US7368065B2 (en) * 2005-06-23 2008-05-06 Depuy Products, Inc. Implants with textured surface and methods for producing the same
US7901462B2 (en) * 2005-06-23 2011-03-08 Depuy Products, Inc. Implants with textured surface and methods for producing the same
WO2007051221A1 (en) * 2005-11-04 2007-05-10 Craig Mclachlan Substrate for tissue growth
EP3517137A1 (en) * 2005-11-14 2019-07-31 Biomet 3I, LLC Deposition of discrete nanoparticles on an implant surface
US20070123923A1 (en) * 2005-11-30 2007-05-31 Lindstrom Curtis C Implantable medical device minimizing rotation and dislocation
US8070821B2 (en) * 2005-12-27 2011-12-06 Howmedica Osteonics Corp. Hybrid femoral implant
WO2007095549A2 (en) 2006-02-13 2007-08-23 Medtronic, Inc. Medical devices having textured surfaces
EP2043561B1 (en) 2006-06-30 2016-01-27 Smith & Nephew, Inc. Anatomical motion hinged prosthesis
WO2008023708A1 (en) * 2006-08-22 2008-02-28 Mitsubishi Electric Corporation Laser processing apparatus, method of bone junction, implant member, process for producing implant member, and implant member production apparatus
US7972648B2 (en) * 2006-10-24 2011-07-05 Biomet 3I, Llc Deposition of discrete nanoparticles on a nanostructured surface of an implant
NL1032851C2 (en) * 2006-11-10 2008-05-14 Fondel Finance B V Kit and method for fixing a prosthesis or part thereof and / or filling bony defects.
US20080154378A1 (en) * 2006-12-22 2008-06-26 Warsaw Orthopedic, Inc. Bone implant having engineered surfaces
US20100137996A1 (en) 2007-05-01 2010-06-03 Moximed, Inc. Femoral and tibial base components
US8894714B2 (en) 2007-05-01 2014-11-25 Moximed, Inc. Unlinked implantable knee unloading device
US20110245928A1 (en) 2010-04-06 2011-10-06 Moximed, Inc. Femoral and Tibial Bases
US20080275567A1 (en) * 2007-05-01 2008-11-06 Exploramed Nc4, Inc. Extra-Articular Implantable Mechanical Energy Absorbing Systems
US7678147B2 (en) * 2007-05-01 2010-03-16 Moximed, Inc. Extra-articular implantable mechanical energy absorbing systems and implantation method
US10022154B2 (en) * 2007-05-01 2018-07-17 Moximed, Inc. Femoral and tibial base components
US8066770B2 (en) * 2007-05-31 2011-11-29 Depuy Products, Inc. Sintered coatings for implantable prostheses
US20090010990A1 (en) * 2007-06-20 2009-01-08 Little Marisa A Process for depositing calcium phosphate therapeutic coatings with controlled release rates and a prosthesis coated via the process
US9993337B1 (en) * 2007-07-19 2018-06-12 Osteosymbionics, Llc Orthopaedic implant and method of making same
US8632600B2 (en) 2007-09-25 2014-01-21 Depuy (Ireland) Prosthesis with modular extensions
US9204967B2 (en) 2007-09-28 2015-12-08 Depuy (Ireland) Fixed-bearing knee prosthesis having interchangeable components
US8828088B2 (en) * 2007-11-08 2014-09-09 Linares Medical Devices, Llc Joint assembly incorporating undercut surface design to entrap accumulating wear debris from plastic joint assembly
US9539097B2 (en) * 2007-11-08 2017-01-10 Linares Medical Devices, Llc Hip and knee joint assemblies incorporating debris collection architecture between the ball and seat interface
US8979938B2 (en) * 2007-11-08 2015-03-17 Linares Medical Devices, Llc Artificial knee implant including liquid ballast supporting / rotating surfaces and incorporating flexible multi-material and natural lubricant retaining matrix applied to a joint surface
GB0724019D0 (en) * 2007-12-08 2008-01-16 Depuy Int Ltd Implant assembly
WO2009097218A1 (en) 2008-01-28 2009-08-06 Biomet 3I, Llc Implant surface with increased hydrophilicity
US20090204213A1 (en) * 2008-02-13 2009-08-13 Depuy Products, Inc. Metallic implants
US8702801B2 (en) * 2008-02-25 2014-04-22 Linares Medical Devices, Llc Artificial wear resistant plug for mounting to existing joint bone
US20090230592A1 (en) * 2008-03-15 2009-09-17 Aubrey Woodroof Laser-Perforated Skin Substitute
WO2009120776A2 (en) * 2008-03-26 2009-10-01 Linares Medical Devices, Llc Joint construction, such as for use by athletes
US8871142B2 (en) * 2008-05-22 2014-10-28 DePuy Synthes Products, LLC Implants with roughened surfaces
US20100042213A1 (en) 2008-08-13 2010-02-18 Nebosky Paul S Drug delivery implants
US9700431B2 (en) 2008-08-13 2017-07-11 Smed-Ta/Td, Llc Orthopaedic implant with porous structural member
US9616205B2 (en) 2008-08-13 2017-04-11 Smed-Ta/Td, Llc Drug delivery implants
US10842645B2 (en) 2008-08-13 2020-11-24 Smed-Ta/Td, Llc Orthopaedic implant with porous structural member
US8475505B2 (en) 2008-08-13 2013-07-02 Smed-Ta/Td, Llc Orthopaedic screws
EP2341852B1 (en) 2008-08-29 2018-08-15 SMed-TA/TD, LLC Orthopaedic implant
WO2010059583A1 (en) * 2008-11-21 2010-05-27 Corning Incorporated Spaced projection substrates and devices for cell culture
JP5404342B2 (en) * 2009-01-06 2014-01-29 キヤノン株式会社 Optical scanning device and image forming apparatus using the same
US8454707B2 (en) * 2009-04-03 2013-06-04 University Of Maryland Biomedical implantable material and methods of producing the same
US8696759B2 (en) * 2009-04-15 2014-04-15 DePuy Synthes Products, LLC Methods and devices for implants with calcium phosphate
PL2253291T3 (en) * 2009-05-19 2016-09-30 A bone implant with a surface anchoring structure
US11213397B2 (en) 2009-05-21 2022-01-04 Depuy Ireland Unlimited Company Prosthesis with surfaces having different textures and method of making the prosthesis
US9101476B2 (en) * 2009-05-21 2015-08-11 Depuy (Ireland) Prosthesis with surfaces having different textures and method of making the prosthesis
US9655731B2 (en) * 2009-08-26 2017-05-23 Zimmer Gmbh Tibial component with enhanced radial cement fixation
US9861408B2 (en) 2009-08-27 2018-01-09 The Foundry, Llc Method and apparatus for treating canine cruciate ligament disease
US9278004B2 (en) 2009-08-27 2016-03-08 Cotera, Inc. Method and apparatus for altering biomechanics of the articular joints
US9668868B2 (en) 2009-08-27 2017-06-06 Cotera, Inc. Apparatus and methods for treatment of patellofemoral conditions
US9795410B2 (en) 2009-08-27 2017-10-24 Cotera, Inc. Method and apparatus for force redistribution in articular joints
US10349980B2 (en) 2009-08-27 2019-07-16 The Foundry, Llc Method and apparatus for altering biomechanics of the shoulder
US8481303B2 (en) 2009-10-12 2013-07-09 Corning Incorporated Microfluidic device for cell culture
US8523948B2 (en) 2009-10-20 2013-09-03 Moximed, Inc. Extra-articular implantable mechanical energy absorbing assemblies having a tension member, and methods
US8679178B2 (en) 2009-10-20 2014-03-25 Moximed, Inc. Extra-articular implantable mechanical energy absorbing assemblies having two deflecting members and compliance member
CH702192A1 (en) * 2009-11-04 2011-05-13 New Dent Ag A ceramic implant.
US8376877B1 (en) * 2009-12-02 2013-02-19 Callaway Golf Company Method and golf club
US8641418B2 (en) 2010-03-29 2014-02-04 Biomet 3I, Llc Titanium nano-scale etching on an implant surface
US9228785B2 (en) 2010-05-04 2016-01-05 Alexander Poltorak Fractal heat transfer device
US8926705B2 (en) 2010-05-10 2015-01-06 Linares Medical Devices, Llc Implantable joint assembly featuring debris entrapment chamber subassemblies along with opposing magnetic fields generated between articulating implant components in order to minimize frictional force and associated wear
JP5951608B2 (en) 2010-08-12 2016-07-13 スミス アンド ネフュー インコーポレーテッド Structures used to fix orthopedic implants and methods of attachment to bone
US8727203B2 (en) 2010-09-16 2014-05-20 Howmedica Osteonics Corp. Methods for manufacturing porous orthopaedic implants
CN102548270A (en) * 2010-12-27 2012-07-04 鸿富锦精密工业(深圳)有限公司 Texture structure, texture method and electronic device with texture structure
US9044270B2 (en) 2011-03-29 2015-06-02 Moximed, Inc. Apparatus for controlling a load on a hip joint
US9012803B2 (en) 2011-09-16 2015-04-21 Ut-Battelle, Llc Method of varying a physical property of a material through its depth
US9381112B1 (en) 2011-10-06 2016-07-05 William Eric Sponsell Bleb drainage device, ophthalmological product and methods
US8771354B2 (en) 2011-10-26 2014-07-08 George J. Picha Hard-tissue implant
US8992619B2 (en) 2011-11-01 2015-03-31 Titan Spine, Llc Microstructured implant surfaces
US20140324186A1 (en) * 2011-11-15 2014-10-30 B6 Sigma, Inc. Medical Implants with Enhanced Osseointegration
US9179954B2 (en) 2011-11-23 2015-11-10 Vivex Biomedical, Inc. Bone screw fastener
US8535388B2 (en) 2011-11-23 2013-09-17 Timothy Ganey Bone graft
US8414654B1 (en) 2011-11-23 2013-04-09 Amendia, Inc. Bone implants and method of manufacture
US8632489B1 (en) 2011-12-22 2014-01-21 A. Mateen Ahmed Implantable medical assembly and methods
WO2013142480A1 (en) 2012-03-20 2013-09-26 Titan Spine, Llc Friction-fit spinal endplate and endplate-preserving method
ES2671740T3 (en) 2012-03-20 2018-06-08 Biomet 3I, Llc Treatment surface for an implant surface
US9468466B1 (en) 2012-08-24 2016-10-18 Cotera, Inc. Method and apparatus for altering biomechanics of the spine
BE1020866A4 (en) * 2012-08-28 2014-06-03 Gaetan Borremans LEGIE.
EP2716261A1 (en) 2012-10-02 2014-04-09 Titan Spine, LLC Implants with self-deploying anchors
US9498349B2 (en) 2012-10-09 2016-11-22 Titan Spine, Llc Expandable spinal implant with expansion wedge and anchor
US9949837B2 (en) 2013-03-07 2018-04-24 Howmedica Osteonics Corp. Partially porous bone implant keel
US9408699B2 (en) 2013-03-15 2016-08-09 Smed-Ta/Td, Llc Removable augment for medical implant
US9724203B2 (en) 2013-03-15 2017-08-08 Smed-Ta/Td, Llc Porous tissue ingrowth structure
US9681966B2 (en) 2013-03-15 2017-06-20 Smed-Ta/Td, Llc Method of manufacturing a tubular medical implant
ITMI20132154A1 (en) * 2013-12-20 2015-06-21 Adler Ortho S R L FEMORAL COMPONENT FOR KNEE PROSTHESIS.
US9615935B2 (en) 2014-01-30 2017-04-11 Titan Spine, Llc Thermally activated shape memory spring assemblies for implant expansion
EP3777753A1 (en) 2014-04-11 2021-02-17 Biomet 3I, LLC Implant with high primary stability and accelerated secondary stability
WO2015200266A1 (en) * 2014-06-23 2015-12-30 Community Blood Center Cellular-scale surface modification for increased osteogenic protein expression
US9649200B2 (en) * 2014-07-28 2017-05-16 Wasaw Orthopedic, Inc. Spinal implant system and method
US10070962B1 (en) 2015-02-13 2018-09-11 Nextstep Arthropedix, LLC Medical implants having desired surface features and methods of manufacturing
JP2016214369A (en) * 2015-05-15 2016-12-22 恭久 高橋 Fixture
WO2017123724A1 (en) * 2016-01-12 2017-07-20 Smed-Ta/Td, Llc Orthopaedic implants with textured porous surfaces
US9975372B2 (en) * 2016-06-21 2018-05-22 Charles White Multi-dimensional art works and methods
US10830545B2 (en) 2016-07-12 2020-11-10 Fractal Heatsink Technologies, LLC System and method for maintaining efficiency of a heat sink
ES2903424T3 (en) * 2016-11-10 2022-04-01 Nantoh Co Ltd Biological Tissue Adhering Surface, Implant, Biological Tissue Adhering Surface Forming Method, and Implant Manufacturing Method
US11406502B2 (en) 2017-03-02 2022-08-09 Optimotion Implants LLC Orthopedic implants and methods
US10905436B2 (en) 2017-03-02 2021-02-02 Optimotion Implants, Llc Knee arthroplasty systems and methods
WO2018165400A1 (en) 2017-03-10 2018-09-13 Applied Medical Research, Inc. Hard-tissue implant comprising a bulk implant, a face, pillars, slots, and at least one support member
US11324606B2 (en) 2017-03-10 2022-05-10 Gary A. Zwick Spinal interbody cage comprising a bulk interbody cage, a top face, a bottom face, pillars, and slots
JP6893838B2 (en) * 2017-07-12 2021-06-23 日本ピストンリング株式会社 Implant surface structure and method of manufacturing implant surface structure
WO2019023476A1 (en) 2017-07-26 2019-01-31 Optimotion Implants LLC Modular knee prosthesis, instruments, and methods
US10499966B2 (en) 2017-10-24 2019-12-10 DePuy Synthes Products, Inc. Bone fixation system including an implant having a plate portion and a mesh portion
US11278427B2 (en) 2018-04-10 2022-03-22 Gary A. Zick, Trustee Of The Everest Trust Uta April 20, 2017 Spinal interbody cage comprising top and bottom faces with mesh structures, pillars and slots
EP3697556A4 (en) * 2018-06-13 2020-09-23 Rize, Inc. Separation of near net shape manufactured parts from support structures
WO2020222035A1 (en) * 2019-04-30 2020-11-05 Universidade Do Minho Dental implant, process of obtention and uses thereof
US11925393B2 (en) * 2019-06-28 2024-03-12 K2M, Inc. Pedicle screw rasp system and adjuster
US11123173B2 (en) 2019-09-11 2021-09-21 Gary A. Zwick Implant comprising first and second sets of pillars for attaching a tendon or a ligament to a hard tissue
AU2021402907A1 (en) 2020-12-18 2023-07-20 Spine Wave, Inc. Expandable tlif device and related insertion and grafting instrumentation

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5645740A (en) * 1993-11-01 1997-07-08 Naiman; Charles S. System and assemblage for producing microtexturized substrates and implants
US5853561A (en) * 1997-06-23 1998-12-29 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Method for surface texturing titanium products
US5965006A (en) * 1996-04-10 1999-10-12 Sulzer Orthopaedie Ag Method for producing a metal surface
US6008431A (en) * 1995-08-29 1999-12-28 Johnson & Johnson Professional, Inc. Bone prosthesis with protected coating for penetrating bone intergrowth
US6235125B1 (en) * 1994-10-06 2001-05-22 Xomed Surgical Products, Inc. Industrial cleaning sponge
US6261322B1 (en) * 1998-05-14 2001-07-17 Hayes Medical, Inc. Implant with composite coating

Family Cites Families (132)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US852873A (en) 1905-11-06 1907-05-07 John B Davidson Steel for sharpening knives.
US3045321A (en) 1955-04-15 1962-07-24 Buckbee Mears Co Abrading devices and method of making them
US3359192A (en) 1965-03-12 1967-12-19 Balco Filtertechnik Gmbh Process of manufacturing a sieve plate having apertures of nonuniform crosssection
US3558310A (en) 1967-03-29 1971-01-26 Rca Corp Method for producing a graphic image
US3605123A (en) 1969-04-29 1971-09-20 Melpar Inc Bone implant
US3679500A (en) 1970-08-07 1972-07-25 Dainippon Screen Mfg Method for forming perforations in metal sheets by etching
US3905080A (en) 1972-03-24 1975-09-16 Buckbee Mears Co Abrading devices
US4033831A (en) 1973-01-05 1977-07-05 Dynamics Research Corporation Method of making a bi-metal screen for thick film fabrication
US4069085A (en) 1973-07-16 1978-01-17 U.S. Philips Corporation Apparatus for forming apertures in a thin metal tape such as a shadow mask for a color television display tube
FR2356465A1 (en) 1976-07-02 1978-01-27 Benoist Girard & Cie PROCESS FOR MANUFACTURING PARTS WITH A GRENUE SURFACE AND PART OBTAINED, IN PARTICULAR SURGICAL PROSTHESES
US4284468A (en) 1977-12-16 1981-08-18 Llewelyn Stearns Patterned chemical etching of high temperature resistant metals
CH630251A5 (en) 1978-05-19 1982-06-15 Sulzer Ag SURFACE STRUCTURE ON ANCHORING ELEMENT OF A BONE IMPLANT.
SE416175B (en) 1979-03-07 1980-12-08 Per Ingvar Branemark FOR IMPLANTATION IN BODY TISSUE Separate Bone Tissue, Dedicated Material
US4422465A (en) 1980-10-17 1983-12-27 Shiseido Company, Ltd. Nail file and method for producing the same
US4644942A (en) 1981-07-27 1987-02-24 Battelle Development Corporation Production of porous coating on a prosthesis
US4834756A (en) 1982-02-18 1989-05-30 Pfizer Hospital Products Group, Inc. Bone prosthesis with porous coating
JPS58151477A (en) 1982-03-02 1983-09-08 Nippon Tenshiyashi Kk Manufacture of metallic polishing body
JPS58204176A (en) 1982-05-24 1983-11-28 Kangiyou Denki Kiki Kk Chemical etching method
US4528070A (en) 1983-02-04 1985-07-09 Burlington Industries, Inc. Orifice plate constructions
GB8318483D0 (en) 1983-07-08 1983-08-10 Zimmer Deloro Surgical Ltd Skeletal implants
US4846839A (en) 1984-02-09 1989-07-11 Joint Medical Products Corporation Apparatus for affixing a prosthesis to bone
EP0159510B1 (en) 1984-04-14 1990-05-30 HOWMEDICA INTERNATIONAL, INC. Zweigniederlassung Kiel Hip joint endoprosthesis
US4673409A (en) 1984-04-25 1987-06-16 Minnesota Mining And Manufacturing Company Implant with attachment surface
US4608052A (en) 1984-04-25 1986-08-26 Minnesota Mining And Manufacturing Company Implant with attachment surface
US4632726A (en) 1984-07-13 1986-12-30 Bmc Industries, Inc. Multi-graded aperture mask method
US4863475A (en) 1984-08-31 1989-09-05 Zimmer, Inc. Implant and method for production thereof
JPS6160889A (en) 1984-08-30 1986-03-28 Toshiba Corp Production of shadow mask
SE450623B (en) 1984-11-07 1987-07-13 Dan Lundgren ELEMENTS OF CONTROLLED TISSUE INVESTMENT IN SURGICAL INTERVENTIONED AREAS
CH665348A5 (en) 1985-01-09 1988-05-13 Sulzer Ag IMPLANTS.
US4634603A (en) 1985-04-22 1987-01-06 United Technologies Corporation Method of abrasive cleaning and spray coating
US4725334A (en) 1985-05-15 1988-02-16 Chem-Tronics, Inc. Method of forming integrally stiffened structures
FR2590275B1 (en) 1985-11-19 1992-07-17 Commissariat Energie Atomique PROCESS FOR PREPARING THE SURFACE OF A PART MADE OF AN URANIUM AND TITANIUM ALLOY, IN PARTICULAR FOR CHEMICAL NICKELING
WO1987005038A1 (en) 1986-02-17 1987-08-27 Commonwealth Scientific And Industrial Research Or Implantable materials
US4714470A (en) 1986-02-19 1987-12-22 Zimmer, Inc. Grooved prosthetic implant
US4871366A (en) 1986-05-27 1989-10-03 Clemson University Soft tissue implants for promoting tissue adhesion to same
US5002572A (en) 1986-09-11 1991-03-26 Picha George J Biological implant with textured surface
GB2199626B (en) 1987-01-08 1991-09-04 Core Vent Corp Screw-type dental implant anchor
SE464394B (en) 1987-05-15 1991-04-22 Sandvik Ab EASY TOOL PLATE FOR PREPARATION AND METHOD FOR PREPARING THEREOF
GB2206614B (en) 1987-07-10 1991-10-16 Nippon Tenshashi Kk Metallic slip-proof element
US4836837A (en) 1987-11-16 1989-06-06 Owens-Corning Fiberglas Corporation Metal coated glass fibers
US5002575A (en) 1988-02-01 1991-03-26 Orthomet, Inc. Bone implant prosthesis
US4851008A (en) 1988-02-01 1989-07-25 Orthomet, Inc. Bone implant prosthesis with substantially stress-free outer surface
US4865603A (en) 1988-02-04 1989-09-12 Joint Medical Products Corporation Metallic prosthetic devices having micro-textured outer surfaces
US4900387A (en) 1988-02-24 1990-02-13 The Boeing Company Method of bonding via electrorheological adhesives
US5139528A (en) 1988-02-26 1992-08-18 Sulzer Brothers Limited Method of securing a mesh to a metal substrate for a bone implant
CH674615A5 (en) 1988-02-26 1990-06-29 Sulzer Ag
JPH0651913B2 (en) 1988-04-22 1994-07-06 川崎製鉄株式会社 Rolling roll surface processing method, apparatus therefor, press working thin metal plate manufactured by the method, and method for manufacturing the same
US5593409A (en) * 1988-06-13 1997-01-14 Sofamor Danek Group, Inc. Interbody spinal fusion implants
CH675826A5 (en) 1988-08-24 1990-11-15 Sulzer Ag
US5011494A (en) 1988-09-16 1991-04-30 Clemson University Soft tissue implant with micron-scale surface texture to optimize anchorage
US5219361A (en) 1988-09-16 1993-06-15 Clemson University Soft tissue implant with micron-scale surface texture to optimize anchorage
US4978358A (en) 1988-10-06 1990-12-18 Zimmer Inc. Orthopaedic prosthetic device possessing improved composite stem design
US5002580A (en) 1988-10-07 1991-03-26 Pfizer Hospital Products Group, Inc. Prosthetic device and method of implantation
DE3836040A1 (en) 1988-10-19 1990-04-26 Mecron Med Prod Gmbh METHOD FOR PRODUCING A PROSTHESIS
US4955909A (en) 1989-01-31 1990-09-11 Bioplasty, Inc. Textured silicone implant prosthesis
ES2044211T3 (en) 1989-03-23 1994-01-01 Straumann Inst Ag METALLIC IMPLANT.
USH788H (en) 1989-05-31 1990-06-05 The United States Of America As Represented By The Secretary Of The Air Force Method for bonding plastic to metal
US4900398A (en) * 1989-06-19 1990-02-13 General Motors Corporation Chemical milling of titanium
US5236459A (en) 1989-09-06 1993-08-17 Sulzer Brothers Limited Bone implant and method of making same
JPH03139821A (en) 1989-10-25 1991-06-14 Toshiba Corp Forming method for micro pattern
GB8925380D0 (en) 1989-11-09 1989-12-28 Leonard Ian Producing prostheses
US5246530A (en) 1990-04-20 1993-09-21 Dynamet Incorporated Method of producing porous metal surface
US5007931A (en) 1990-05-04 1991-04-16 Boehringer Mannheim Corporation Porous coated prosthesis
DE59103876D1 (en) 1990-09-13 1995-01-26 Thera Ges Fuer Patente Implantable prosthesis.
US6008430A (en) 1991-01-30 1999-12-28 Interpore Orthopaedics, Inc. Three-dimensional prosthetic articles and methods for producing same
US5312456A (en) 1991-01-31 1994-05-17 Carnegie Mellon University Micromechanical barb and method for making the same
US5271736A (en) 1991-05-13 1993-12-21 Applied Medical Research Collagen disruptive morphology for implants
US5258098A (en) 1991-06-17 1993-11-02 Cycam, Inc. Method of production of a surface adapted to promote adhesion
US5207709A (en) 1991-11-13 1993-05-04 Picha George J Implant with textured surface
GB9202248D0 (en) 1992-02-03 1992-03-18 Howmedica Prosthesis for attachement without bone cement and method of attaching
US5358533A (en) 1992-02-19 1994-10-25 Joint Medical Products Corporation Sintered coatings for implantable prostheses
CA2074425C (en) * 1992-06-25 2003-01-07 Daniel M. Wyner Multi-layered sheet
US5268068A (en) 1992-12-08 1993-12-07 International Business Machines Corporation High aspect ratio molybdenum composite mask method
US5307594A (en) 1992-12-14 1994-05-03 Zimmer, Inc. Method for forming textured surfaces on an orthopaedic implant
US5294567A (en) * 1993-01-08 1994-03-15 E. I. Du Pont De Nemours And Company Method for forming via holes in multilayer circuits
US5486234A (en) * 1993-07-16 1996-01-23 The United States Of America As Represented By The United States Department Of Energy Removal of field and embedded metal by spin spray etching
ES2149194T3 (en) * 1993-08-18 2000-11-01 Sulzer Orthopadie Ag PROCEDURE FOR FORMING ANCHORAGE SURFACES IN OUTLET ON JOINT IMPLANTS.
JP3282347B2 (en) 1993-09-07 2002-05-13 ソニー株式会社 Etching method, color selection mechanism and manufacturing method thereof, and cathode ray tube
JP2764526B2 (en) 1993-09-28 1998-06-11 大日本印刷株式会社 Manufacturing method of aperture grill and aperture grill
SE504294C2 (en) 1993-10-01 1996-12-23 Lucocer Ab Implants intended to be fixed by contact with newly formed bone tissue
US6419491B1 (en) * 1993-11-02 2002-07-16 Bio-Lok International, Inc. Dental implant system with repeating microgeometric surface patterns
US20010039454A1 (en) 1993-11-02 2001-11-08 John Ricci Orthopedic implants having ordered microgeometric surface patterns
US5607480A (en) 1993-11-10 1997-03-04 Implant Innovations, Inc. Surgically implantable prosthetic devices
DE4403509A1 (en) * 1994-02-04 1995-08-10 Draenert Klaus Material and process for its manufacture
US5665118A (en) 1994-02-18 1997-09-09 Johnson & Johnson Professional, Inc. Bone prostheses with direct cast macrotextured surface regions and method for manufacturing the same
CA2142636C (en) 1994-02-18 2005-09-20 Salvatore Caldarise Implantable articles with as-cast macrotextured surface regions and method of manufacturing the same
GB2288537B (en) 1994-04-12 1997-11-12 Corin Medical Ltd A prosthesis component
US5484074A (en) 1994-05-03 1996-01-16 Bmc Industries, Inc. Method for manufacturing a shadow mask
JP3457675B2 (en) * 1994-05-24 2003-10-20 テクノロジィ ファイナンス コーポレイション (プロプライエタリー)リミテッド Biocompatible materials and bone implants for bone repair and replacement
JPH07320652A (en) 1994-05-27 1995-12-08 Toshiba Corp Manufacture of color picture tube and shadow mask
CH689725A5 (en) 1994-09-08 1999-09-30 Franz Dr Sutter Condyle prosthesis.
US5571017A (en) 1994-10-05 1996-11-05 Core-Vent Corporation Selective surface, externally-threaded endosseous dental implant
GB9420071D0 (en) 1994-10-05 1994-11-16 Howmedica Metal backing for inclusion in the manufacture of a prosthetic component
TW378334B (en) 1994-10-14 2000-01-01 Thomson Consumer Electronics Method of forming an enhanced resolution shadow mask
EP1488760B1 (en) 1994-11-30 2010-03-31 Biomet 3i, LLC Implant surface preparation
JP3450920B2 (en) * 1994-12-26 2003-09-29 京セラ株式会社 Method for manufacturing bioprosthesis member
US6051751A (en) * 1995-01-20 2000-04-18 Spire Corporation Arthroplasty process for securely anchoring prostheses to bone, and arthroplasty products therefor
AU5095196A (en) 1995-03-17 1996-10-08 Smith & Nephew Richards Inc. Medical implants
US5606589A (en) 1995-05-09 1997-02-25 Thermo Trex Corporation Air cross grids for mammography and methods for their manufacture and use
US6149688A (en) 1995-06-07 2000-11-21 Surgical Dynamics, Inc. Artificial bone graft implant
US5639237A (en) 1995-06-08 1997-06-17 Fontenot; Mark G Dental prosthesis having indentations
US5944517A (en) * 1995-07-28 1999-08-31 J.P. Winkelstroeter Kg, Dentaurum Dental appliance to be worn in the mouth, in particular in the form of a bracket
US6149689A (en) 1995-11-22 2000-11-21 Eska Implants Gmbh & Co. Implant as bone replacement
ATE235927T1 (en) * 1996-05-10 2003-04-15 Isotis Nv DEVICE FOR RECEIVING AND RELEASING BIOLOGICALLY ACTIVE SUBSTANCES
US6143948A (en) * 1996-05-10 2000-11-07 Isotis B.V. Device for incorporation and release of biologically active agents
US6171344B1 (en) * 1996-08-16 2001-01-09 Children's Medical Center Corporation Bladder submucosa seeded with cells for tissue reconstruction
US5843250A (en) 1996-08-19 1998-12-01 High Tech Polishing, Inc. Method of forming an image pattern on a die plate
US5716412A (en) 1996-09-30 1998-02-10 Johnson & Johnson Professional, Inc. Implantable article with ablated surface
CN1186874A (en) 1996-12-31 1998-07-08 财团法人韩国机械研究院 Method for manufacturing engraved rolling rool and apparatus for manufacturing the same
KR19980061912A (en) 1996-12-31 1998-10-07 서상기 METHOD FOR MANUFACTURING ROLLS AND ROLLS
US5728159A (en) 1997-01-02 1998-03-17 Musculoskeletal Transplant Foundation Serrated bone graft
US5997580A (en) * 1997-03-27 1999-12-07 Johnson & Johnson Professional, Inc. Cement restrictor including shape memory material
US6120539A (en) * 1997-05-01 2000-09-19 C. R. Bard Inc. Prosthetic repair fabric
US5876457A (en) * 1997-05-20 1999-03-02 George J. Picha Spinal implant
US6106558A (en) * 1997-09-15 2000-08-22 Applied Medical Research, Inc. Neuro decompression device
EP0904751B1 (en) * 1997-09-30 2003-08-20 Centerpulse Orthopedics Ltd. Tubular support body for bridging two vertebrae
US6008432A (en) 1997-10-01 1999-12-28 Osteonics Corp. Metallic texture coated prosthetic implants
US5975903A (en) 1998-04-02 1999-11-02 Shoher; Edan C. Dental implant and implant system
EP1152718A1 (en) * 1999-02-04 2001-11-14 SDGI Holdings, Inc. Improved interbody fusion device with anti-rotation features
US6235638B1 (en) * 1999-02-16 2001-05-22 Micron Technology, Inc. Simplified etching technique for producing multiple undercut profiles
US6095817A (en) * 1999-02-24 2000-08-01 Sulzer Calcitek Inc. Dental implant having multiple textured surfaces
TW593770B (en) 1999-05-10 2004-06-21 Air Prod & Chem Method for anisotropic etching of copper thin films with a beta-diketone, a beta-ketoimine, or a breakdown product thereof
US6312612B1 (en) 1999-06-09 2001-11-06 The Procter & Gamble Company Apparatus and method for manufacturing an intracutaneous microneedle array
US6277150B1 (en) * 1999-06-11 2001-08-21 Gore Enterprise Holdings, Inc. Facial implant having one porous surface
US6221109B1 (en) * 1999-09-15 2001-04-24 Ed. Geistlich Söhne AG fur Chemische Industrie Method of protecting spinal area
TW491714B (en) * 1999-12-08 2002-06-21 Wen-Jing Shiue Orthopedic implant having a porous surface and method of making same
EP1279697A4 (en) * 1999-12-10 2006-06-28 Yupo Corp Porous resin film
US6217333B1 (en) * 2000-05-09 2001-04-17 Carlo Ercoli Dental implant for promoting reduced interpoximal resorption
DE10108153A1 (en) * 2000-09-28 2002-10-24 Henkel Kgaa Tray tablets and process for their manufacture
US7087200B2 (en) * 2001-06-22 2006-08-08 The Regents Of The University Of Michigan Controlled local/global and micro/macro-porous 3D plastic, polymer and ceramic/cement composite scaffold fabrication and applications thereof
US7238203B2 (en) * 2001-12-12 2007-07-03 Vita Special Purpose Corporation Bioactive spinal implants and method of manufacture thereof
WO2004002373A2 (en) * 2002-06-27 2004-01-08 Ferree Bret A Arthroplasty devices for improved bone ingrowth

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5645740A (en) * 1993-11-01 1997-07-08 Naiman; Charles S. System and assemblage for producing microtexturized substrates and implants
US6235125B1 (en) * 1994-10-06 2001-05-22 Xomed Surgical Products, Inc. Industrial cleaning sponge
US6008431A (en) * 1995-08-29 1999-12-28 Johnson & Johnson Professional, Inc. Bone prosthesis with protected coating for penetrating bone intergrowth
US5965006A (en) * 1996-04-10 1999-10-12 Sulzer Orthopaedie Ag Method for producing a metal surface
US5853561A (en) * 1997-06-23 1998-12-29 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Method for surface texturing titanium products
US6261322B1 (en) * 1998-05-14 2001-07-17 Hayes Medical, Inc. Implant with composite coating

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009000774A1 (en) * 2007-06-22 2008-12-31 Societa' Azionaria Materiale Ospedaliero - S.A.M.O. S.P.A. Method for producing surfaces for metal articles
EP2286767A1 (en) * 2009-08-21 2011-02-23 Jossi Holding AG Method for producing a structured surface on a workpiece from a metallic material and implant with such a surface

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