510(k) K960303 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
FENNING FEMORAL COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 21, 1996 |
| Received | Jan 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960303
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.