510(k) K932210 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, Sep 7, 1994 |
| Received | May 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932210
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.