510(k) K212023 ยท OLO Orthopedic Stereotaxic Instrument
Virage Navigation System
| Applicant | Zimmer Biomet Spine, Inc., Westminister CO, US |
| Decision | Substantially Equivalent, Aug 27, 2021 |
| Received | Jun 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212023
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.