510(k) K232116 ยท OLO Orthopedic Stereotaxic Instrument
CoreLink Navigation Instruments
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Aug 16, 2023 |
| Received | Jul 17, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232116
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.