510(k) K925900 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
LACEY REVISION FEMORAL COMPONENT
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent, Aug 24, 1993 |
| Received | Nov 20, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925900
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.