510(k) K031901 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
PROVEN REVISION FEMORAL AND PROVEN REVISION TIBIAL INSERT
| Applicant | Stelkast Company, Mcmurray PA, US |
| Decision | Substantially Equivalent, Oct 10, 2003 |
| Received | Jun 20, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031901
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.