510(k) K253266 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Titanium Interbody System
| Applicant | Spine Innovation, LLC, Coronado CA, US |
| Decision | Substantially Equivalent, Jan 8, 2026 |
| Received | Sep 29, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K253266
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.