510(k) K830121 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
INSALL/BURSTEIN FIBER METAL CONDYLAR/KNE
| Applicant | Zimmer, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 26, 1983 |
| Received | Jan 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830121
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 20, 2014 | Zimmer, Inc. I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGII KNEE SLF-TAP BONE ST Terminated |
JWH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.