510(k) K960302 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
CONSENSUS ACETABULAR SHELL, ALL UHMWPE
| Applicant | U.S. Medical Products, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Apr 1, 1996 |
| Received | Jan 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960302
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.