510(k) K961793 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
BI-LOC BIPOLAR CUP
| Applicant | Ortho Development Corp., Draper UT, US |
| Decision | Substantially Equivalent, Jul 26, 1996 |
| Received | May 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961793
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.