510(k) K241716 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee Component
| Applicant | Howmedica Osteonics Corp., Dba Stryker Orthopaedics, Mahwah NJ, US |
| Decision | Substantially Equivalent, Aug 2, 2024 |
| Received | Jun 14, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241716
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.