510(k) K203742 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
IdentiTi ALIF Standalone Interbody System
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, Apr 9, 2021 |
| Received | Dec 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203742
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.