510(k) K152621 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
OSS/Arcos IM Total Femur Rod
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 14, 2015 |
| Received | Sep 14, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152621
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.