510(k) K922048 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
DURACON ALL PLASTIC TIBIAL COMPONENT
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Sep 8, 1992 |
| Received | May 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922048
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.