510(k) K893959 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
P.S.A. FEMORAL HIP PROSTHESIS
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jul 25, 1989 |
| Received | Jun 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893959
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.