510(k) K962086 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
CPS, CEMENTED CUP SYSTEM
| Applicant | Artos Medical Products GmbH, Indianapolis IN, US |
| Decision | Substantially Equivalent, Aug 7, 1996 |
| Received | May 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962086
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.