510(k) K954138 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
DURACON MONOLITHIC STABILIZER FEMORAL COMPONENT
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent for Some Indications, Nov 21, 1995 |
| Received | Sep 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954138
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.