510(k) K050441 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
TAPER 2 POROUS FEMORAL STEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 29, 2005 |
| Received | Feb 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050441
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.