510(k) K241375 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IdentiTi Porous Ti Interbody System; IdentiTi NanoTec Interbody System; IdentiTi Cervical Porous Ti Interbody System; IdentiTi NanoTec Cervical Interbody System; IdentiTi Cervical Standalone Interbody System; IdentiTi NanoTec Cervical Standalone Interbody System; IdentiTi ALIF Standalone Interbody S
| Applicant | Alphatec Spine, Carlsbad CA, US |
| Decision | Substantially Equivalent, Feb 3, 2025 |
| Received | May 15, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241375
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.