510(k) K791823 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
3M UPF PROXIMAL FEMUR REPLACEMENT SYSTEM
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, Oct 30, 1979 |
| Received | Sep 14, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791823
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.