510(k) K920231 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
OMNIFIT M-HA HIP STEM SERIES
| Applicant | Stryker Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Jun 8, 1992 |
| Received | Jan 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920231
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.