|Publication number||US3562820 A|
|Publication date||Feb 16, 1971|
|Filing date||Aug 21, 1967|
|Priority date||Aug 22, 1966|
|Also published as||DE1617330B1|
|Publication number||US 3562820 A, US 3562820A, US-A-3562820, US3562820 A, US3562820A|
|Original Assignee||Bernhard Braun|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (194), Classifications (19) |
|External Links: USPTO, USPTO Assignment, Espacenet|
Tubular sheet and strip form prostheses on a basis of biological tissue
US 3562820 A
Feb. 16, 1971 BRUN TUBULAR SHEET AND STRIP FORM PROSTHESES ON A BASIS OF BIOLOGICAL TISSUE Filed Aug. 21, 1967 WIIIIIIIIIIIIIIII FIG. 2
INVENTOR BERNHARD BRAUN Maf pl? ATTORNEYS.
United States Patent 3,562,820 TUBULAR SHEET AND STRIP FORM PROSTHESES ON A BASIS OF BIOLOGICAL TISSUE Bernhard Braun, Trankeiucke 1, Melsungen, Germany Filed Aug. 21, 1967, Ser. No. 661,900 Claims priority, application Austria, Aug. 22, 1966, A 7,958/66 Int. Cl. A61f 1/24 US. Cl. 3-1 5 Claims ABSTRACT OF THE DISCLOSURE There are disclosed tubular, sheet and strip form prostheses on a basis of biological tissue for use in the replacement, repair and strengthening of various living organs such as the vasculature, esophagus, bronchus, intestine, ureter, liver, kidney, etc. and a process for making and using the same. The prosthesis itself comprises a unitary structure of alternating layers of natural tissue and collagen fibres. The same is manufactured by applying a strip, sheet or tube of biological material onto a substantially rigid support, coating the exposed surface with a binder paste, as for example, a collagen fibre paste, or bringing about the swelling of the exposed surface, thereafter applying a second layer of natural material and repeating the procedure until the desired Wall thickness is obtained. The multi-layer prosthesis is then dried and removed from the underlying support.
The invention described herein relates to tubular, strip and sheet form prostheses on a basis of biological tissue and to methods for manufacturing and using the same. More particularly this invention relates to a multi-layer prosthesis on a basis of biological tissue.
The prostheses of the invention are suitable for use as vascular, esophagus, bronchus, intestinal, ureter and cardiac valve prostheses and as other corrective parts of various organs such as liver.
It is already known to prepare tubes and fabrics from polytetrafluoroethylene or polyester fibers, either by weaving or knitting or by a combined weaving and knitting process and to use the same to replace diseased blood vessels or parts of the heart. At first, clinical results with these prostheses were satisfactory and highly promising, but deterioration set in after some considerable time (Materia Medica Nordmark 16, , page 245 and Der Internist 6  H. 5, page 216). Among the other disadvantages which were observed, for example, was that natural tissue did not grow into the synthetic fibre fabric. To overcome this disadvantage it has been proposed to make the synthetic fibre fabrics in a more open mesh, but this impaired other properties of the prostheses, for example, the strength thereof. A further disadvantage associated with the known synthetic fibre prostheses is the difliculty encountered in suturing the same into position because the synthetic fiber prostheses tear easily and the holes thus formed do not close.
The present invention overcomes the difficulties above mentioned and provides a prosthetic device for use in the replacement, repair and strengthening of living organs superior in effectiveness to anything previously known.
One of the objects of the invention is the provision of a prosthesis that is created from biological tissue which does not undergo deterioration after installation even after prolonged periods.
Another object is the provision of a prosthesis that is created from biological tissue that will allow for and facilitate tissue growth and organ regeneration at the site of installation.
Patented Feb. 16, 1971 A further object is the provision of a prosthesis that is created from biological tissue which can be simply and effectively installed using the conventional techniques.
Still a further object of the invention is the provision of a method by which such a prosthesis on a basis of biological tissue can be formed.
The manner in which these and other objects of this invention are obtained will become apparent from the detailed description and the following drawings in which:
FIG. 1 is a longitudinal central section through an embodiment of a prosthesis in accordance with the invention;
FIG. 2 is a diagrammatic view illustrating the method of forming the prosthesis of FIG. 1; and
FIGS. 3 and 4 are diagrammatic perspective views illustrating two somewhat different forms of the prostheses embodying the invention.
According to the invention there is provided a prosthesis in tubular, sheet or strip form which comprises at least two layers of biological tissue intimately joined and dried. More specific-ally the prosthesis comprises alternating layers of biological tissue and collagen fibers intimately joined and dried.
According to the present invention, the biological prostheses are manufactured by placing over, i.e., applying onto the surface of a firm support a piece of tubular, sheet or strip form biological tissue, causing the exposed surface thereof to swell so as to produce thereon an adhesive or glue like effect and/ or the exposed surface is coated with a binder or bonding agent as for example a collagen fiber paste, a second piece of biological tissue is then applied to the first and the procedure repeated until a multi-layered structure of the desired wall thickness is obtained. The prosthesis is then dried and removed from the support.
As natural tissue for use in the manufacture of the prostheses of the invention there are suitable in particular the submucosa, which can be obtained in pure form from the small intestine of sheep, goats and other animals, and the so-called goldbeaters skin, which is made up of the serosa taken from the intestines of cattle. The submucosa, which is obtained in the form of a fine, but high strength tube, is composed of diagonally disposed collagen fibres. The mucosa and muscular tissue still adhering to the submucosa can easily be removed by the process as conventionally used in the manufacture of catgut.
As the strength of a single layer of submucoca is far too inadequate, the same having a thickness of only about 15 1,, it is advantageous to use a number of layers cemented together with a binder, as for example, a collagen fibre paste. The collagen fibre paste may be prepared, for example, by the process described in German patent specification No. 659,490. Furthermore, this layer of collagen fibres ensures that any holes, tears, and the like made in the tissue during the manufacture thereof, during the operation for installing the same, or a later time, will close easily. This can prevent hemorrhage, which hitherto has been highly dangerous. The collagen fibre paste has a further advantage in that therapeutic substances may be incorporated therein. Thus, for example, heparin may be added to inhibit the clotting of blood, cartilage powder or chondroitin sulfate included to stimulate the formation of new collagen fibres for the vascular intima, as Well as other therapeutic substances.
It is also possible to cause the individual layers of tissue to swell and to bond them together in the swollen state. Organic acids, especially dilute lactic acid, have been found to be particularly suitable for swelling the single layers. The use of highly dilute solutions of lactic acid is preferred in this connection as the same has the advantage that no acidic end products are formed.
In carrying out the process of the invention it is possible to use, for example, a tubular core or a plate made of glass or a synthetic material as the firm, more or less rigid support. Instances of synthetic materials include polyolefins as for example polyethylene or polypropylene etc. However, any inert fairly firm material may be employed. Prior to use, it is advantageous to treat the surface or surfaces of the support with a lubricant, as for example, glycerol or a silicone oil. A thoroughly cleansed tubular or flat piece of biological tissue, for example, submucosa or serosa tissue, which may have been subjected to bleaching with hydrogen peroxide, is then placed onto the support. The tissue is then coated with a binder paste, preferably a collagen fibre paste, and, if necessary, the paste is allowed to dry slightly. Another piece of tissue is then applied, and the process is repeated until the desired thickness is obtained. The finished prosthesis may contain, for example, about eight layers of tissue. The number of layers is generally determined by the thickness of the composite layers and by the ultimate use.
The prosthesis made by the process of the invention may be subjected to a hardening process to prevent premature absorption by the body tissues. As hardening agents there may be used physiologically acceptable vegetable or synthetic substances or, as for example, aldehydes. Instances of aldehydes that are suitable for this purpose are formaldehyde, glutardialdehyde and aldehydes of higher polyhydroxy compounds. The concentration of the hardening agent may be varied to produce the rate of absorption required.
The hardening process is preferably carried out after the final layer of tissue has been applied. However, it is possible to harden the single layers of tissue before they are applied. By adopting this latter procedure, the single layers of tissue may be hardened to varying degrees, thereby producing a prosthesis in which the single layers have different rates of absorption. For example, when using a tubular core as a support, the innermost layers may be hardened to a considerable degree to produce a tough, resistant core, and the outside layers may be only slightly hardened to ensure a specific rate of absorption.
After removal of the support and, if necessary, after the tube has been cut open, fascia prostheses are obtained which are generally known as patches and which may be used to close defects in the tympanic membrane and the heart wall, for hollow-walled organs or as heart valves.
Furthermore, collagen patches in sheet form are also used to repair damage to parenchymatous soft tissue, for example, in the liver, kidney, spleen and pancreas. This can be effected in the following manner:
A so-called mattress suture is made, i.e., a large atrau matic needle threaded with a soft suture is passed through the parenchymatous tissue on one side of the wound and out of the other side. The needle is then passed through a stiffened and perforated collagen patch from underneath. The needle is then passed back through an adjacent perforation in the collagen patch at an appropriate distance from the point at which it emerged, through the organ and out the other side. The length of the suture should be such that a second perforated collagen patch may be threaded onto the two ends. When the needle has been removed, the two ends of the suture are knotted together over the collagen patch.
Strips for surgical purposes, as for example, for securing a movable kidney or for use in surgery of the incontinentia vesicae, may also be cut from sheets, i.e., membranes of the same material.
Tubular, flat or fluted prostheses may also be made by the process of the invention in addition to membranes and strips. The tubular prostheses may be of uniform diameter throughout their length or their diameter may be widened or narrowed conically.
Referring to the drawing a tube made of synthetic material as, for example, a tube made of polyethylene or polypropylene and which has been provided with a plurality of threads 2 is thoroughly cleaned and, if necessary, treated with a silicone oil. A tube of tissue 3, preferably submucosa, which has been thoroughly cleansed and, if necessary, bleached With hydrogen peroxide, is drawn over the polyethylene tube 1, allowed to dry slightly, if necessary, and then a synthetic filament 4 is wound round the tubular tissue corresponding to the depressions of the thread and the tissue is dried. The filament may then be removed. The submucosa 3 is thus provided with a thread 2' and is of a standardized size. The tissue is then coated with a binder paste, preferably a collagen fibre paste, the paste is allowed to dry slightly, and then another tube of tissue is drawn over the first one. A synthetic filament is wound round it as before and the tissue is dried. This procedure may be repeated until the desired thickness of wall is obtained. The multiple layers of tissue are firmly cemented together by the binder. When the single layers of tissue are to be united by swelling it is possible either first to swell the single layers of tissue and to draw them onto the tube or core in the swollen state or to swell them on the core. To free the tube formed by these layers of tissue from the supporting tube or core, warm air is passed through the tube or core in this case a plastic tube, to soften it slightly, whereupon both ends of the tube are pulled until it stretches and detaches from the tissue at the beginning of the thread section. It can then be pulled out of the submucosa tube in the form of a plastic filament without the submucosa tube adhering to it or being damaged. Prostheses suitable for various purposes may be produced by varying the pitch of the thread, the depth of the thread and the number of turns.
The threaded tube of tissue so obtained has the necessary strength, density and elasticity required of vascular prostheses, and it can be sutured and is puncture-proof. The thread with which it is provided prevents it from kinking when it is moved after implantation in the host, thereby permitting an unhindered flow of blood. It is also extensible.
On the other hand, if a smooth tubular prosthesis is required, that is to say, without any thread or fluting, for example, as used for prosthetic repair of the cystic duct, the ureter, the esophagus or, in special cases, blood vessels, the same procedure as with the screw-threaded plastic tube may be followed, but without winding a filament round the tissue or allowing it to conform to the shape of the thread. The elastic tube of tissue is drawn over the plastic tube and held taut over it by tying the tissue tube at both ends and allowing it to conform to the outer circumference of the plastic tube without complementing the shape of the thread. Alternatively, a smooth plastic tube may be used as a support, for the layers of tissue.
Prostheses, for example, for the esophagus, trachea and intestine, can be made by the process described above, with due regard to anatomical requirements, diameter and thickness of wall. The strength of such prostheses can be considerably increased by placing layers of synthetic or natural tissue or even metallic clasps or spirals between the layers making up the actual prosthesis. The synthetic tissue used may be made, for example, from polyamide or polyester fibres. The natural tissue may be, for example, biological tissue, for exam ple, serosa tissue, or material made from natural fibres. The serosa tissue may be wound round the prosthesis diagonally, first from left to right and then from right to left. If necessary, these layers of tissue may be pretreated, as for example, by stretching.
It is also possible to bond the layers of tissue by swelling the tubular or flat pieces in an acidic or alkaline medium. In this process the upper layers of collagen fibers are slightly hydrolyzed and converted into tropocollagen which, on drying, has a glue-like adhesive effect.
The process has a negative effect on the physical properties of the collagen fibre and neutralization is generally necessary afterwards, followed by washing out of the salts formed during neutralization.
Sterilization of the prostheses so obtained may be elfected by gamma-radiation, which process also reduces the antigenic properties of the collagen.
In FIGS. 3 and 4 there are shown two somewhat ditferent forms of the prostheses in accordance with the invention. In FIG. 3 the embodiment comprising alternating layers of biological tissue 7 bonded together with a bond ing agent 8 is shown and in FIG. 4 the embodiment wherein the bonding is effected by swelling the layers 7 is set out.
The prostheses in accordance with the invention has been subjected to trial and has been observed and evaluated as a suitability, production of toxic symptoms, decomposition, detachment, secondary reactions such as abnormal tissue growth, etc. The trials consisted in surgical implantation of the prostheses in otherwise normal animals, i.e., the requirement for the prostheses was surgically induced, observation of the thusly treated animals during the recovery period and for varying periods thereafter. During this time, numerous test procedures were carried out, the same including chemical, X-ray, electrocardiographic, etc., procedures. At the end of various predetermined time intervals certain of the animals were sacrificed and any of the animals possibly involved organs examined both microscopically and macroscopically. In every instance, the results of procedures and tests in both the living and sacrificed animals established the safety and suitability of the prosthetic devices for replacement and repair of damaged organs. It is to be noted that as experimental animals, there were employed cats, dogs and monkeys.
The device has been surgically implanted in human subjects, in each case where the subjects condition was indicative of such treatment. Almost all of the subjects are still under observation and to date there have not been observed any untoward results or happenings directly associated with the use of the herein disclosed prosthetic devices.
What is claimed is:
1. A tubular prosthetic device on a basis of biological tissue comprising at least two superimposed layers consisting of tubes of natural tissue applied in their natural tubular form prepared from the submucous layers of intestines of mammals, and said layers being bonded together by means of collagen fibers.
2. A prosthetic device according to claim 1 wherein said collagen fibres consist of a collagen fiber paste.
3. A prosthetic device according to claim 1 wherein at least one of said layers is a prehardened layer which has been prehardened by contacting the same with a hardening agent.
4. A prosthetic device according to claim 3 wherein said hardening agent is an aldehyde.
5. A hardened prosthetic device according to claim 1 wherein said prosthetic device has been hardened by treatment thereof with a hardening agent.
References Cited UNITED STATES PATENTS 1,254,031 l/1918 Davis 128-3355 2,127,903 8/1938 Bowen 128334 3,272,204 9/1966 Artandi et a1. 128-334 3,366,440 1/1968 Nuwayser 128-334X 3,425,418 2/ 1969 Chvapil et al 128334 OTHER REFERENCES Experimental and Clinical Utilization of a Prosthesis for Replacement of the Trachea, by R. E. Taber et al., A.M.A. Archives of Surgery, vol. 77, October 1958, pp. 576-583. I
DALTON L. TRULUCK, Primary Examiner R. L. FRINKS, Assistant Examiner US. Cl. X.R.
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3866609 *||Jun 11, 1973||Feb 18, 1975||Charles Howard Sparks||Apparatus for growing graft tubes in place|
|US3894530 *||Jul 6, 1973||Jul 15, 1975||Herbert Dardik||Method for repairing, augmenting, or replacing a body conduit or organ|
|US3974526 *||Jan 23, 1975||Aug 17, 1976||Dardik Irving I||Vascular prostheses and process for producing the same|
|US3988782 *||Apr 1, 1975||Nov 2, 1976||Dardik Irving I||Non-antigenic, non-thrombogenic infection-resistant grafts from umbilical cord vessels and process for preparing and using same|
|US3993078 *||Nov 3, 1975||Nov 23, 1976||Gambro Ag||Insert for use preferably in vascular surgery|
|US4014971 *||May 11, 1973||Mar 29, 1977||Perkins Rodney C||Method for making a tympanic membrane prosthesis|
|US4061134 *||Oct 28, 1975||Dec 6, 1977||Samuels Peter B||Arterial graft device|
|US4077069 *||Jan 14, 1977||Mar 7, 1978||Perkins Rodney C||Synthetic tympanic membrane|
|US4130904 *||Jun 6, 1977||Dec 26, 1978||Thermo Electron Corporation||Prosthetic blood conduit|
|US4483339 *||Feb 29, 1984||Nov 20, 1984||Rolando Gillis||Vascular surgery roll|
|US4553974 *||Aug 14, 1984||Nov 19, 1985||Mayo Foundation||Treatment of collagenous tissue with glutaraldehyde and aminodiphosphonate calcification inhibitor|
|US4629458 *||Feb 26, 1985||Dec 16, 1986||Cordis Corporation||Reinforcing structure for cardiovascular graft|
|US4676790 *||Sep 25, 1985||Jun 30, 1987||Kern Seymour P||Method of manufacture and implantation of corneal inlays|
|US4759758 *||Dec 7, 1984||Jul 26, 1988||Shlomo Gabbay||Prosthetic heart valve|
|US4772283 *||Dec 9, 1987||Sep 20, 1988||White Thomas C||Corneal implant|
|US4787899 *||Dec 10, 1986||Nov 29, 1988||Lazarus Harrison M||Intraluminal graft device, system and method|
|US4798606 *||Aug 27, 1986||Jan 17, 1989||Corvita Corporation||Reinforcing structure for cardiovascular graft|
|US4842599 *||Nov 12, 1987||Jun 27, 1989||Ann M. Bronstein||Prosthetic cornea and method of implantation therefor|
|US4850999 *||May 26, 1981||Jul 25, 1989||Institute Fur Textil-Und Faserforschung Of Stuttgart||Flexible hollow organ|
|US4902508 *||Jul 11, 1988||Feb 20, 1990||Purdue Research Foundation||Tissue graft composition|
|US4956178 *||Nov 6, 1989||Sep 11, 1990||Purdue Research Foundation||Tissue graft composition|
|US5282823 *||Mar 19, 1992||Feb 1, 1994||Medtronic, Inc.||Intravascular radially expandable stent|
|US5443496 *||Oct 15, 1993||Aug 22, 1995||Medtronic, Inc.||Intravascular radially expandable stent|
|US5514176 *||Jan 20, 1995||May 7, 1996||Vance Products Inc.||Pull apart coil stent|
|US5573784 *||Apr 18, 1995||Nov 12, 1996||Methodist Hospital Of Indiana, Inc.||Graft for promoting autogenous tissue growth|
|US5628788 *||Nov 7, 1995||May 13, 1997||Corvita Corporation||Self-expanding endoluminal stent-graft|
|US5645860 *||Apr 16, 1996||Jul 8, 1997||Methodist Hospital Of Indiana, Inc.||Tissue graft and method for urinary urothelium reconstruction replacement|
|US5651174 *||Apr 27, 1995||Jul 29, 1997||Medtronic, Inc.||Intravascular radially expandable stent|
|US5662700 *||Nov 18, 1994||Sep 2, 1997||Endovascular Technologies, Inc.||Artificial graft and implantation method|
|US5700269 *||Nov 13, 1995||Dec 23, 1997||Corvita Corporation||Endoluminal prosthesis deployment device for use with prostheses of variable length and having retraction ability|
|US5711969 *||Apr 7, 1995||Jan 27, 1998||Methodist Hospital Of Indiana||Large area submucosal tissue graft constructs|
|US5714582 *||Mar 17, 1995||Feb 3, 1998||Bioscience Consultants||Invertebrate type V telopeptide collagen, methods of making, and use thereof|
|US5733337 *||Apr 7, 1995||Mar 31, 1998||Organogenesis, Inc.||Tissue repair fabric|
|US5741333 *||Apr 3, 1996||Apr 21, 1998||Corvita Corporation||Self-expanding stent for a medical device to be introduced into a cavity of a body|
|US5755791 *||Apr 5, 1996||May 26, 1998||Methodist Hospital Of Indiana||Perforated submucosal tissue graft constructs|
|US5762966 *||Jan 15, 1997||Jun 9, 1998||Methodist Hospital Of Indiana||Tissue graft and method for urinary tract urothelium reconstruction and replacement|
|US5785679 *||Jul 19, 1995||Jul 28, 1998||Endotex Interventional Systems, Inc.||Methods and apparatus for treating aneurysms and arterio-venous fistulas|
|US5788625 *||Apr 5, 1996||Aug 4, 1998||Depuy Orthopaedics, Inc.||Method of making reconstructive SIS structure for cartilaginous elements in situ|
|US5849037 *||Apr 3, 1996||Dec 15, 1998||Corvita Corporation||Self-expanding stent for a medical device to be introduced into a cavity of a body, and method for its preparation|
|US5858556 *||Jan 21, 1997||Jan 12, 1999||Uti Corporation||Multilayer composite tubular structure and method of making|
|US5865723 *||Dec 29, 1995||Feb 2, 1999||Ramus Medical Technologies||Method and apparatus for forming vascular prostheses|
|US5873906 *||Jul 21, 1997||Feb 23, 1999||Gore Enterprise Holdings, Inc.||Procedures for introducing stents and stent-grafts|
|US5876432 *||Mar 28, 1995||Mar 2, 1999||Gore Enterprise Holdings, Inc.||Self-expandable helical intravascular stent and stent-graft|
|US5879383 *||Jun 30, 1997||Mar 9, 1999||W. L. Gore & Associates, Inc.||Blood contact surfaces using endothelium on a subendothelial matrix|
|US5885619 *||Sep 16, 1997||Mar 23, 1999||Methodist Hospital Of Indiana, Inc.||Large area submucosal tissue graft constructs and method for making the same|
|US5911757 *||Jun 7, 1995||Jun 15, 1999||Seare, Jr.; William J.||Methods and apparatus for transcutaneous access|
|US5919225 *||Jul 14, 1997||Jul 6, 1999||Gore Enterprise Holdings, Inc.||Procedures for introducing stents and stent-grafts|
|US5922028 *||Oct 16, 1997||Jul 13, 1999||Depuy Orthopaedics, Inc.||Multi-layered SIS tissue graft construct for replacement of cartilaginous elements in situ|
|US5925061 *||Jan 13, 1997||Jul 20, 1999||Gore Enterprise Holdings, Inc.||Low profile vascular stent|
|US5955110 *||Apr 5, 1996||Sep 21, 1999||Methodist Hospital Of Indiana, Inc.||Multilayered submucosal graft constructs and method for making the same|
|US5968091 *||Nov 26, 1997||Oct 19, 1999||Corvita Corp.||Stents and stent grafts having enhanced hoop strength and methods of making the same|
|US5968096 *||Aug 6, 1997||Oct 19, 1999||Clarian Health Partners||Method of repairing perforated submucosal tissue graft constructs|
|US5997575 *||Sep 18, 1997||Dec 7, 1999||Methodist Hospital Of Indiana, Inc.||Perforated submucosal tissue graft constructs|
|US6001123 *||May 28, 1996||Dec 14, 1999||Gore Enterprise Holdings Inc.||Folding self-expandable intravascular stent-graft|
|US6015429 *||Mar 12, 1996||Jan 18, 2000||Gore Enterprise Holdings, Inc.||Procedures for introducing stents and stent-grafts|
|US6017362 *||Jan 22, 1997||Jan 25, 2000||Gore Enterprise Holdings, Inc.||Folding self-expandable intravascular stent|
|US6017364 *||May 21, 1998||Jan 25, 2000||Endovascular Technologies, Inc.||Intraluminal repair device and catheter|
|US6042605 *||Jul 18, 1997||Mar 28, 2000||Gore Enterprose Holdings, Inc.||Kink resistant stent-graft|
|US6077217 *||Jun 25, 1997||Jun 20, 2000||Ramus Medical Technologies, Inc.||System and method for assembling graft structures|
|US6126686 *||Dec 10, 1997||Oct 3, 2000||Purdue Research Foundation||Artificial vascular valves|
|US6165210 *||Apr 1, 1994||Dec 26, 2000||Gore Enterprise Holdings, Inc.||Self-expandable helical intravascular stent and stent-graft|
|US6176880||Apr 4, 1997||Jan 23, 2001||Depuy Orthopaedics, Inc.||Tissue graft construct for replacement of cartilaginous structures|
|US6187039||Dec 10, 1997||Feb 13, 2001||Purdue Research Foundation||Tubular submucosal graft constructs|
|US6221102||Jun 7, 1995||Apr 24, 2001||Endovascular Technologies, Inc.||Intraluminal grafting system|
|US6237460||Apr 30, 1998||May 29, 2001||Corvita Corporation||Method for preparation of a self-expanding stent for a medical device to be introduced into a cavity of a body|
|US6331188||Jun 9, 1997||Dec 18, 2001||Gore Enterprise Holdings, Inc.||Exterior supported self-expanding stent-graft|
|US6334872||Jul 7, 1997||Jan 1, 2002||Organogenesis Inc.||Method for treating diseased or damaged organs|
|US6337389||Oct 28, 1997||Jan 8, 2002||Bioscience Consultants, L.L.C.||Method and process for the production of collagen preparations from invertebrate marine animals and compositions thereof|
|US6344053||Apr 5, 1999||Feb 5, 2002||Medtronic Ave, Inc.||Endovascular support device and method|
|US6348065||Jul 24, 1998||Feb 19, 2002||Scimed Life Systems, Inc.||Longitudinally flexible expandable stent|
|US6352553||Jul 18, 1997||Mar 5, 2002||Gore Enterprise Holdings, Inc.||Stent-graft deployment apparatus and method|
|US6352561||Dec 23, 1996||Mar 5, 2002||W. L. Gore & Associates||Implant deployment apparatus|
|US6358284 *||Jun 2, 1999||Mar 19, 2002||Med Institute, Inc.||Tubular grafts from purified submucosa|
|US6361637||Aug 13, 1999||Mar 26, 2002||Gore Enterprise Holdings, Inc.||Method of making a kink resistant stent-graft|
|US6416535||Sep 28, 1999||Jul 9, 2002||Endovascular Technologies, Inc.||Artificial graft and implantation method|
|US6494904||Dec 27, 1996||Dec 17, 2002||Ramus Medical Technologies||Method and apparatus for forming vascular prostheses|
|US6517570||Jul 21, 1997||Feb 11, 2003||Gore Enterprise Holdings, Inc.||Exterior supported self-expanding stent-graft|
|US6520986||Jun 26, 2001||Feb 18, 2003||Gore Enterprise Holdings, Inc.||Kink resistant stent-graft|
|US6551350||Dec 23, 1996||Apr 22, 2003||Gore Enterprise Holdings, Inc.||Kink resistant bifurcated prosthesis|
|US6572650||Jun 4, 1999||Jun 3, 2003||Organogenesis Inc.||Bioengineered vascular graft support prostheses|
|US6576265||Oct 18, 2000||Jun 10, 2003||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6579538||Oct 18, 2000||Jun 17, 2003||Acell, Inc.||Tissue regenerative compositions for cardiac applications, method of making, and method of use thereof|
|US6610085||Nov 13, 1996||Aug 26, 2003||Endovascular Technologies, Inc.||Intraluminal repair device and method|
|US6613072||Jul 18, 1997||Sep 2, 2003||Gore Enterprise Holdings, Inc.||Procedures for introducing stents and stent-grafts|
|US6638312||Jul 30, 2001||Oct 28, 2003||Depuy Orthopaedics, Inc.||Reinforced small intestinal submucosa (SIS)|
|US6645342||Mar 8, 2002||Nov 11, 2003||William M. Scott||Pull strip for forming holes|
|US6656219||Nov 22, 2000||Dec 2, 2003||Dominik M. Wiktor||Intravascular stent|
|US6663661||Oct 31, 2001||Dec 16, 2003||Medtronic Ave, Inc.||Endovascular support device and method|
|US6702844||Sep 27, 1999||Mar 9, 2004||Endovascular Technologies, Inc.||Artificial graft and implantation method|
|US6770088||May 18, 2000||Aug 3, 2004||Scimed Life Systems, Inc.||Intravascular stent|
|US6783776||Oct 25, 2002||Aug 31, 2004||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6790220 *||Jun 10, 2002||Sep 14, 2004||Morris Innovative Research, Inc.||Method and apparatus for sealing access|
|US6793676||Jan 23, 2001||Sep 21, 2004||Depuy Orthopaedics, Inc.||Method of reconstructing a joint|
|US6814748||Jun 14, 2002||Nov 9, 2004||Endovascular Technologies, Inc.||Intraluminal grafting system|
|US6818014||Aug 3, 1995||Nov 16, 2004||Scimed Life Systems, Inc.||Longitudinally flexible expandable stent|
|US6827733||Sep 24, 2003||Dec 7, 2004||Medtronic Ave, Inc.||Endovascular support device and method|
|US6846323||May 15, 2003||Jan 25, 2005||Advanced Cardiovascular Systems, Inc.||Intravascular stent|
|US6849273||Oct 25, 2002||Feb 1, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6852339||Oct 25, 2002||Feb 8, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6860901||Jul 2, 2002||Mar 1, 2005||Endovascular Technologies, Inc.||Intraluminal grafting system|
|US6861074||Oct 25, 2002||Mar 1, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6869619||Oct 25, 2002||Mar 22, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6887495||Oct 25, 2002||May 3, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6890351 *||Sep 7, 2001||May 10, 2005||Organogenesis Inc.||Method for treating diseased or damaged organs|
|US6890562||Oct 25, 2002||May 10, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6890563||Oct 25, 2002||May 10, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6890564||Oct 25, 2002||May 10, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6893666||Oct 25, 2002||May 17, 2005||Acell, Inc.||Tissue regenerative composition, method of making, and method of use thereof|
|US6913619||Jul 11, 2002||Jul 5, 2005||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US6916910||Nov 28, 2001||Jul 12, 2005||Bioscience Consultants||Method and process for the production of collagen preparations from invertebrate marine animals and compositions thereof|
|US6923828||Nov 22, 2000||Aug 2, 2005||Medtronic, Inc.||Intravascular stent|
|US6939377||Aug 20, 2001||Sep 6, 2005||Thoratec Corporation||Coated vascular grafts and methods of use|
|US6962603||Jun 22, 2000||Nov 8, 2005||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US6981986||Sep 20, 2000||Jan 3, 2006||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US6986735||Mar 3, 2003||Jan 17, 2006||Organogenesis Inc.||Method of making a bioremodelable vascular graft prosthesis|
|US7041131||Apr 11, 2003||May 9, 2006||Organogenesis, Inc.||Bioengineered vascular graft support prostheses|
|US7060103||Feb 28, 2003||Jun 13, 2006||Organogenesis Inc.||Tissue repair fabric|
|US7070558 *||Jun 12, 2003||Jul 4, 2006||Boston Scientific Scimed, Inc.||Medical slings|
|US7081130||Apr 16, 2002||Jul 25, 2006||Boston Scientific Scimed, Inc.||Intravascular Stent|
|US7121999||Mar 3, 2003||Oct 17, 2006||Organogenesis Inc.||Method of preparing layered graft prostheses|
|US7131992 *||Oct 9, 2002||Nov 7, 2006||Olympus Corporation||Stent|
|US7160326||Oct 29, 2002||Jan 9, 2007||Depuy Products, Inc.||Method and apparatus for implantation of soft tissue implant|
|US7160333||Sep 5, 2003||Jan 9, 2007||Depuy Orthopaedics, Inc.||Reinforced small intestinal submucosa|
|US7163563||Jul 15, 2002||Jan 16, 2007||Depuy Products, Inc.||Unitary surgical device and method|
|US7166125||Oct 10, 2000||Jan 23, 2007||Endovascular Technologies, Inc.||Intraluminal grafting system|
|US7201917||Jul 15, 2002||Apr 10, 2007||Depuy Products, Inc.||Porous delivery scaffold and method|
|US7204848||Nov 20, 1998||Apr 17, 2007||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US7214242||Mar 3, 2003||May 8, 2007||Organogenesis, Inc.||Bioengineered tubular graft prostheses|
|US7326241||Aug 9, 2001||Feb 5, 2008||Boston Scientific Scimed, Inc.||Intravascular stent|
|US7354627||Dec 22, 2004||Apr 8, 2008||Depuy Products, Inc.||Method for organizing the assembly of collagen fibers and compositions formed therefrom|
|US7361195||Jul 15, 2002||Apr 22, 2008||Depuy Products, Inc.||Cartilage repair apparatus and method|
|US7485138||Feb 6, 2002||Feb 3, 2009||Cook Biotech Incorporated||Tubular graft construct|
|US7513866||Oct 29, 2004||Apr 7, 2009||Depuy Products, Inc.||Intestine processing device and associated method|
|US7550004||Mar 30, 2005||Jun 23, 2009||Cook Biotech Incorporated||Endoluminal device with extracellular matrix material and methods|
|US7569233||Apr 20, 2005||Aug 4, 2009||Depuy Products, Inc.||Hybrid biologic-synthetic bioabsorbable scaffolds|
|US7595062||Jul 28, 2005||Sep 29, 2009||Depuy Products, Inc.||Joint resurfacing orthopaedic implant and associated method|
|US7652077 *||Mar 26, 2004||Jan 26, 2010||Cook Incorporated||Graft prosthesis, materials and methods|
|US7682380||Jul 1, 2002||Mar 23, 2010||Gore Enterprise Holdings, Inc.||Kink-resistant bifurcated prosthesis|
|US7699895||Dec 23, 2003||Apr 20, 2010||Cook Biotech Incorporated||Multi-formed collagenous biomaterial medical device|
|US7713552||Dec 19, 2001||May 11, 2010||Cook Biotech Incorporated||Radiopaque implantable collagenous biomaterial device|
|US7766956||Nov 26, 2003||Aug 3, 2010||Boston Scientific Scimed, Inc.||Intravascular stent and assembly|
|US7799089||Oct 10, 2006||Sep 21, 2010||Depuy Orthopaedics, Inc.||Reinforced small intestinal submucosa|
|US7819918||Dec 29, 2003||Oct 26, 2010||Depuy Products, Inc.||Implantable tissue repair device|
|US7833267 *||Oct 24, 2008||Nov 16, 2010||Cook Incorporated||Methods and systems for modifying vascular valves|
|US7857825||Nov 20, 2003||Dec 28, 2010||Cook Biotech Incorporated||Embolization device|
|US7871440||Dec 11, 2006||Jan 18, 2011||Depuy Products, Inc.||Unitary surgical device and method|
|US7887576||May 19, 2009||Feb 15, 2011||Cook Incorporated||Endoluminal device with extracellular matrix material and methods|
|US7909886||Mar 24, 2006||Mar 22, 2011||Organogenesis, Inc.||Tissue repair fabric|
|US7914808||Jul 15, 2002||Mar 29, 2011||Depuy Products, Inc.||Hybrid biologic/synthetic porous extracellular matrix scaffolds|
|US7972385 *||Sep 25, 2006||Jul 5, 2011||Antonio Sambusseti||Patch for replacement of a portion of bladder wall following partial cystectomy|
|US7988717||Nov 10, 2003||Aug 2, 2011||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US7988720||Jul 20, 2007||Aug 2, 2011||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US7993365||Jun 8, 2004||Aug 9, 2011||Morris Innovative, Inc.||Method and apparatus for sealing access|
|US8007542||Oct 31, 2007||Aug 30, 2011||Cook Biotech Incorporated||Freeze-dried collagenous biomaterial medical sponge device|
|US8012205||Jul 15, 2002||Sep 6, 2011||Depuy Products, Inc.||Cartilage repair and regeneration device|
|US8021414||Jul 25, 2002||Sep 20, 2011||Boston Scientific Scimed, Inc.||Intravascular stent|
|US8025896||Jul 15, 2002||Sep 27, 2011||Depuy Products, Inc.||Porous extracellular matrix scaffold and method|
|US8070792||Mar 28, 2002||Dec 6, 2011||Boston Scientific Scimed, Inc.||Stent|
|US8092529||Jul 15, 2002||Jan 10, 2012||Depuy Products, Inc.||Meniscus regeneration device|
|US8109995||Aug 8, 2008||Feb 7, 2012||Colibri Heart Valve Llc||Percutaneously implantable replacement heart valve device and method of making same|
|US8114146||Mar 15, 2004||Feb 14, 2012||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US8118832||Jun 15, 2009||Feb 21, 2012||Morris Innovative, Inc.||Method and apparatus for sealing access|
|US8128708||Jan 28, 2010||Mar 6, 2012||Cook Biotech Incorporated||Multi-formed collagenous biomaterial medical device for use in wound care|
|US8142489||Sep 5, 2008||Mar 27, 2012||Boston Scientific Scimed, Inc.||Flexible and expandable stent|
|US8257715||Aug 24, 2005||Sep 4, 2012||University Of Notre Dame||Tissue vaccines and uses thereof|
|US8298586||Jul 22, 2009||Oct 30, 2012||Acell Inc||Variable density tissue graft composition|
|US8308797||Jul 10, 2004||Nov 13, 2012||Colibri Heart Valve, LLC||Percutaneously implantable replacement heart valve device and method of making same|
|US8323328||Sep 9, 2002||Dec 4, 2012||W. L. Gore & Associates, Inc.||Kink resistant stent-graft|
|US8337537 *||Jul 15, 2002||Dec 25, 2012||Depuy Products, Inc.||Device from naturally occurring biologically derived materials|
|US8348992||Aug 21, 2001||Jan 8, 2013||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US8361144||Mar 1, 2011||Jan 29, 2013||Colibri Heart Valve Llc||Percutaneously deliverable heart valve and methods associated therewith|
|US8366787 *||Jun 14, 2002||Feb 5, 2013||Depuy Products, Inc.||Hybrid biologic-synthetic bioabsorbable scaffolds|
|US8388643||Aug 5, 2005||Mar 5, 2013||The Regents Of The University Of California||Bioabsorbable polymeric implants and a method of using the same to create occlusions|
|US8409625||Jan 9, 2009||Apr 2, 2013||Acell, Inc.||Conditioned decellularized native tissues for tissue restoration|
|US8439942||Dec 3, 2010||May 14, 2013||Cook Bioteck Incorporated||Embolization device|
|US8449597||Nov 21, 2011||May 28, 2013||Boston Scientific Scimed, Inc.||Longitudinally flexible expandable stent|
|US8449607||Jul 26, 2012||May 28, 2013||Cormatrix Cardiovascular, Inc.||Prosthetic tissue valve|
|US8541032||Oct 11, 2012||Sep 24, 2013||Acell, Inc.||Tissue graft composition|
|US8562665||Dec 17, 2002||Oct 22, 2013||Boston Scientific Scimed, Inc.||Tubular stent consists of chevron-shape expansion struts and contralaterally attached diagonal-connectors|
|US8623065||Oct 7, 2002||Jan 7, 2014||W. L. Gore & Associates, Inc.||Exterior supported self-expanding stent-graft|
|US20100076555 *||Sep 15, 2009||Mar 25, 2010||Marten Lewis H||Coated devices comprising a fiber mesh imbedded in the device walls|
|DE2422383A1 *||May 9, 1974||Nov 21, 1974||Rodney C Perkins||Synthetische anatomische glieder und verfahren zu deren herstellung|
|EP0965310A1 *||Dec 2, 1997||Dec 22, 1999||SHIMIZU, Yasuhiko||Artificial blood vessel|
|EP1177800A1 *||Jul 31, 2001||Feb 6, 2002||Depuy Orthopaedics, Inc.||Reinforced small intestinal submucosa|
|EP1985320A1||May 27, 1999||Oct 29, 2008||Cook Biotech, Inc.||A multi-formed collagenous biomaterial medical device|
|WO1984003036A1 *||Jan 26, 1984||Aug 16, 1984||Wallsten Hans Ivar||Blood vessel prosthesis|
|WO1987001930A1 *||Sep 19, 1986||Apr 9, 1987||Seymour P Kern||Method of manufacture and implantation of corneal inlays|
|WO1990000395A1 *||Jun 23, 1989||Jan 25, 1990||Purdue Research Foundation||Tissue graft composition and method|
|WO1996031226A1 *||Apr 5, 1996||Oct 10, 1996||Stephen F Badylak||Large area submucosal graft constructs and method for making the same|
|WO1997037613A1 *||Apr 4, 1997||Oct 16, 1997||Depuy Orthopaedics Inc||Tissue graft construct for replacement of cartilaginous structures|
|WO2006135297A1 *||Mar 28, 2006||Dec 21, 2006||Sinova Safetech Innovation Ab||Bowel implant|
|WO2007147739A2 *||Jun 7, 2007||Dec 27, 2007||Orthomed||Collagen tubes|
|WO2008134541A2 *||Apr 25, 2008||Nov 6, 2008||Musculoskeletal Transplant||Reinforced biological mesh for surgical reinforcement|
|WO2009040768A2 *||Sep 25, 2008||Apr 2, 2009||Carlos Alvarado||Tissue grafting method|
| || |
|U.S. Classification||623/23.64, 8/94.18, 156/308.6, 156/83, 8/94.11, 428/473, 156/326, 428/35.6|
|International Classification||A61L27/36, A61F2/00, A61F2/06, A61L27/24|
|Cooperative Classification||A61F2310/00365, A61F2/06, A61L27/3629, A61L27/24|
|European Classification||A61L27/36B12, A61F2/06, A61L27/24|