510(k) K915525 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent, May 5, 1993 |
| Received | Dec 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915525
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.