510(k) K864085 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
BROOKER BIO-GROOVE FEMORAL COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 28, 1987 |
| Received | Oct 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864085
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.