510(k) K913632 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
BATEMAN UPF-III BIPOLAR ENDOPROSTHESIS SYSTEM
| Applicant | Kirschner Medical Corp., Timonium MD, US |
| Decision | Substantially Equivalent, Nov 13, 1991 |
| Received | Aug 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913632
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.