510(k) K925613 ยท KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
PROXIMAL HUMERAL REPLACEMENT SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 14, 1994 |
| Received | Nov 5, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925613
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.