510(k) K213708 · OLO Orthopedic Stereotaxic Instrument
ROSA® Knee System
| Applicant | Orthosoft Inc (D/B/A Zimmer Cas), Montreal, CA |
| Decision | Substantially Equivalent, Apr 22, 2022 |
| Received | Nov 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213708
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.