510(k) K171073 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Smith & Nephew, Inc. REDAPT Augments
| Applicant | Smith & Nephew, Inc., Cordova TN, US |
| Decision | Substantially Equivalent, Nov 21, 2017 |
| Received | Apr 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171073
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.