510(k) K890742 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
INTRAFORM TOTAL HIP SYSTEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent for Some Indications, May 10, 1989 |
| Received | Feb 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890742
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.