510(k) K001374 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
PATIENT MATCHED COBALT ALLOY TROCHLEA REPLACEMENT
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 27, 2000 |
| Received | May 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001374
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.