510(k) K914169 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent, Jan 27, 1992 |
| Received | Sep 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914169
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.