US2009312842A1PendingUtilityA1
Assembled Cartilage Repair Graft
Est. expiryJun 16, 2028(~1.9 yrs left)· nominal 20-yr term from priority
A61F 2002/30138A61F 2002/30332A61F 2002/30883A61F 2230/0093A61F 2230/0069A61F 2220/0025A61F 2230/0017A61F 2230/0065A61F 2/28A61F 2002/302A61F 2002/30485A61F 2/30771A61F 2002/30878A61F 2002/30772A61F 2002/30299A61F 2220/0033A61F 2002/30075A61F 2002/30057A61F 2002/30233A61F 2002/30766A61F 2002/30337A61F 2002/30224A61B 17/86A61F 2/30756A61F 2002/30751A61F 2002/30929
49
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Claims
Abstract
Bifunctional and assembled implants are provided for osteochondral implantation.
Claims
exact text as granted — not AI-modified1 . A bifunctional assembled implant adapted for implantation at a site of a bone cartilage junction, comprising:
an osteoconductive portion adapted to fill a defect in a subchondral bone layer; and a chondroinductive portion adapted to fill a cartilage layer adjacent to the subchondral bone layer; wherein said osteoconductive portion and said chondroinductive portion are derived from different source materials and are assembled in a stacked relationship.
2 . The implant of claim 1 , wherein said osteoconductive portion and said chondroinductive portion each defines a characteristic depth and a characteristic width; and
wherein said characteristic depth of said osteoconductive portion is substantially equivalent to or greater than said characteristic depth of said chondroinductive portion.
3 . The implant of claim 2 , wherein said characteristic depth of said osteoconductive portion is at least about one and one half times greater than said characteristic depth of said chondroinductive portion; and wherein said characteristic width of said osteoconductive portion is substantially the same as said characteristic width of said chondroinductive portion.
4 . The implant of claim 2 , wherein said osteoconductive portion and said chondroinductive portion are assembled to have an interference fit.
5 . The implant of claim 4 , wherein said interference fit is a hydration controlled shrink fit.
6 . The implant of claim 6 , wherein said interference fit further comprises a shaft and bore fit between said osteoconductive portion and said chondroinductive portion, and the shaft is straight or tapered.
7 . The implant of claim 1 , wherein said chondroinductive portion comprises a demineralized cortical bone portion.
8 . The implant of claim 7 , wherein said demineralized cortical bone portion includes one or more canals, said canals being oriented in a direction communicating between said osteoconductive portion and at least one surface of said demineralized cortical bone portion.
9 . The implant of claim 8 , wherein said demineralized cortical bone portion comprises from two to eight pieces of cortical bone
10 . The implant of claim 8 , wherein said osteoconductive portion substantially surrounds at least one part of said chondroinductive portion.
11 . The implant of claim 8 , wherein said demineralized cortical bone portion consists essentially of a single piece of substantially demineralized cortical bone.
12 . The implant of claim 1 , wherein:
said osteoconductive portion consists essentially of cancellous bone, and said chondroinductive portion consists essentially of cortical bone.
13 . The implant of claim 13 , wherein said chondroinductive portion comprises allograft bone, xenograft bone, or a combination thereof.
14 . (canceled)
15 . The implant of claim 12 , wherein said bifunctional assembled implant does not comprise separate fasteners for holding together said osteoconductive portion and said chondroinductive portion.
16 . The implant of claim 12 , wherein said bifunctional assembled implant does not comprise an adhesive for holding together said osteoconductive portion and said chondroinductive portion.
17 . The implant of claim 1 , wherein said osteoconductive portion comprises cancellous bone material and said chondroinductive portion comprises cortical bone material; and wherein said osteoconductive portion and said chondroinductive portion are joined by a hydration controlled shrink fit, and wherein a part of said osteoconductive portion surrounds a part of said chondroinductive portion.
18 . The implant of claim 17 , wherein said cortical bone material further includes one or more canals, said canals being oriented in a direction providing transport between said cancellous bone material and said cortical bone material.
19 . A method of using an assembled osteochondral implant, comprising filling a defect site with said bifunctional assembled implant of claim 1 , such that a first region of said defect site is filled by osteoconductive cancellous bone material and a second region of said defect site is filled by chondroinductive cortical bone material.
20 . An implant adapted for implantation at an articulating cartilage site, comprising a membrane of demineralized cortical bone, wherein the membrane has a thickness, a length and a width, and wherein said thickness is less than said length and said width, and wherein the membrane includes natural Haversian canals oriented generally perpendicular to the thickness of said membrane.
21 - 24 . (canceled)
25 . A method of making a bifunctional assembled implant adapted for implantation at the site of a bone cartilage junction, comprising:
providing an osteoconductive portion adapted to fill a defect in a subchondral bone layer; and assembling said osteoconductive portion with a chondroinductive portion adapted to fill a corresponding cartilage layer; wherein said osteoconductive portion and said chondroinductive portion are assembled via an interference fit.
26 - 32 . (canceled)Join the waitlist — get patent alerts
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