510(k) K253583 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LUX Expandable Lumbar Interbody System
| Applicant | Xenix Medical, Orlando CA, US |
| Decision | Substantially Equivalent, Feb 23, 2026 |
| Received | Nov 17, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253583
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.