510(k) K220973 ยท OLO Orthopedic Stereotaxic Instrument
CoreLink Navigation Instruments
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 1, 2022 |
| Received | Apr 4, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220973
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.