510(k) K950202 ยท KWZ Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
RINGLOC CONSTRAINED LINER
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, May 15, 1995 |
| Received | Jan 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950202
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.