510(k) K251969 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Atlas Spine Project X Expandable Posterior Lumbar Interbody System
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Aug 15, 2025 |
| Received | Jun 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251969
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.