510(k) K061340 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
23 MM SINGLE-PEG PATELLA COMPONENT
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 25, 2006 |
| Received | May 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061340
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.