510(k) K922008 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
CDH HIP SYSTEM
| Applicant | Howmedica, Pfizer Medical Technology Group, Rutherford NJ, US |
| Decision | Substantially Equivalent, Jul 30, 1992 |
| Received | Apr 30, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922008
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.