510(k) K262646 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Calibrate MAX System; Calibrate NanoTec MAX System; Calibrate CCX Interbody System; Calibrate NanoTec CCX Interbody System
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 21, 2026 |
| Received | Jul 30, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262646
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.