510(k) K874740 ยท JDG Prosthesis, Hip, Femoral Component, Cemented, Metal
WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, Dec 18, 1987 |
| Received | Nov 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874740
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.