510(k) K920739 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
S-ROM TOTAL HIP REPLACEMENT SYSTEM
| Applicant | Joint Medical Products Corp., Stamford CT, US |
| Decision | Substantially Equivalent for Some Indications, Nov 24, 1992 |
| Received | Feb 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920739
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.