510(k) K152169 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Balanced Knee System TriMax CR Femoral Component and E-Vitalize CR and UC Tibial Inserts
| Applicant | Ortho Development Corporation, Draper UT, US |
| Decision | Substantially Equivalent, Oct 27, 2015 |
| Received | Aug 4, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152169
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.