510(k) K920639 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
RX 90 ACETABULAR COMPONENT SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 30, 1992 |
| Received | Feb 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920639
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.