510(k) K964795 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
CEMENTED CALCAR REPLACEMENT FEMORAL STEM
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Feb 19, 1997 |
| Received | Nov 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964795
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.