510(k) K230880 ยท OLO Orthopedic Stereotaxic Instrument
CoreLink Navigation Instruments
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, May 2, 2023 |
| Received | Mar 30, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230880
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.