510(k) K960984 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
SHP HIP SYSTEM-FEMORAL COMPONENTS/ACETABULAR COMPONENTS/MODULAR HEADS/CENTRALIZERS
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 17, 1996 |
| Received | Mar 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960984
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.