510(k) K926323 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
H-110 ACETABULAR CUP SYSTEM
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, May 26, 1993 |
| Received | Dec 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926323
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.