510(k) K920250 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
OSTEONICS MICROSURFACED CDH HIP STEM
| Applicant | Stryker Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 20, 1992 |
| Received | Jan 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920250
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.