510(k) K162962 ยท OLO Orthopedic Stereotaxic Instrument
OrthAlign Plus System
| Applicant | Orthalign, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Jan 23, 2017 |
| Received | Oct 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162962
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.