510(k) K852584 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
POROUS APF/COLLARLESS MODULAR FEMORAL COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 15, 1985 |
| Received | Jun 18, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852584
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.