510(k) K251080 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
IdentiTi II Cervical Interbody System
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jul 3, 2025 |
| Received | Apr 8, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251080
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.