510(k) K151902 · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
REDAPT¿ Revision Femoral System
| Applicant | Smith & Nephew, Inc., Cordova TN, US |
| Decision | Substantially Equivalent, Sep 3, 2015 |
| Received | Jul 10, 2015 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K151902
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.