510(k) K902538 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATION
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, Jul 6, 1990 |
| Received | Jun 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902538
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.