510(k) K170690 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
M-Vizion Femoral Revision System
| Applicant | Medacta International S.A., Castel San Pietro (Ch), CH |
| Decision | Substantially Equivalent, Nov 29, 2017 |
| Received | Mar 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170690
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.