510(k) K023188 ยท KXA Prosthesis, Hip, Femoral, Resurfacing
PRESS-FIT HEAD RESURFACING DEVICE
| Applicant | Biomet Orthopedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 11, 2002 |
| Received | Sep 24, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023188
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.