510(k) K881779 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEM
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, Aug 31, 1988 |
| Received | Apr 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881779
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.