510(k) K123501 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
OSS MODULAR STEMS, OSS DIAPHYSEAL SEGMENTS
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 27, 2013 |
| Received | Nov 13, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123501
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.