510(k) K182731 ยท OLO Orthopedic Stereotaxic Instrument
Corelink Navigation Instruments
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 13, 2019 |
| Received | Sep 28, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182731
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.