510(k) K781294 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
PROSTHESIS, KNEE, TOTAL
| Applicant | Biomet, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Aug 14, 1978 |
| Received | Jul 27, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781294
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.