510(k) K251575 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
IdentiTi II ALIF Standalone Interbody System; Transcend ALIF Standalone Interbody System
| Applicant | Alphatec Spine, Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 3, 2025 |
| Received | May 22, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251575
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.