510(k) K001759 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
HEDROCEL REVISION CUP, MODEL 02-2YY-ZZZZ
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 24, 2000 |
| Received | Jun 9, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001759
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.