510(k) K230567 · SBF Orthopedic Augmented Reality
OptiVu ROSA® MxR
| Applicant | Orthosoft Inc (D/B/A Zimmer Cas), Montreal, CA |
| Decision | Substantially Equivalent, Jun 13, 2023 |
| Received | Mar 1, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230567
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.