510(k) K162921 ยท OLO Orthopedic Stereotaxic Instrument
Navigated Instrument System
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, Mar 13, 2017 |
| Received | Oct 18, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162921
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.