510(k) K963242 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
DURACON POSTERIOR FEMORAL SPACER
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Nov 14, 1996 |
| Received | Aug 19, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963242
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.