510(k) K242364 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IdentiTi II Interbody System
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 4, 2024 |
| Received | Aug 9, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242364
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.