510(k) K253748 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Jan 23, 2026 |
| Received | Nov 25, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253748
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.