510(k) K892398 ยท KXA Prosthesis, Hip, Femoral, Resurfacing
BIPOLAR HIP SYSTEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 23, 1989 |
| Received | Apr 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892398
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.