510(k) K021799 ยท KXA Prosthesis, Hip, Femoral, Resurfacing
CEMENTED FEMORAL HEAD RESURFING DEVICE
| Applicant | Biomet Orthopedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 26, 2002 |
| Received | May 31, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021799
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.