510(k) K883941 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
PROFORMA HIP SYSTEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 30, 1988 |
| Received | Sep 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883941
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.