510(k) K243571 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners
| Applicant | Zimmer Biomet, Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 31, 2025 |
| Received | Nov 18, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243571
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.