510(k) K222028 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IdentiTi Porous Ti Interbody System, IdentiTi NanoTec Interbody System, Transcend PEEK Interbody System, Transcend NanoTec Interbody System, IdentiTi ALIF Standalone Interbody System, IdentiTi NanoTec ALIF Standalone Interbody System
| Applicant | Alphatec Spine, Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 7, 2022 |
| Received | Jul 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222028
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.