510(k) K160923 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
REDAPT Anteverted Cemented Liner
| Applicant | Smith & Nephew, Inc., Cordova TN, US |
| Decision | Substantially Equivalent, Nov 17, 2016 |
| Received | Apr 4, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160923
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.