510(k) K212825 ยท OLO Orthopedic Stereotaxic Instrument
CoreLink Navigation Instruments
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Oct 13, 2021 |
| Received | Sep 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212825
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.