510(k) K864070 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
WHITESIDE ORTHOLOC (TM)
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, Jan 27, 1987 |
| Received | Oct 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864070
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.