510(k) K202812 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
IdentiTi Cervical Standalone Interbody System
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, Dec 18, 2020 |
| Received | Sep 24, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202812
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.