510(k) K260173 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
M-Vizion Femoral Revision System Extension
| Applicant | Medacta International S.A., Castel San Pietro, CH |
| Decision | Substantially Equivalent, Sep 17, 2026 |
| Received | Jan 21, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260173
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.