510(k) K961304 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
AURA HIP SYSTEM CEMENTED FEMORAL STEM/CEMENTED LONG FEMORAL STEM
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Oct 1, 1996 |
| Received | Apr 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961304
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.