510(k) K251502 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Jul 7, 2025 |
| Received | May 15, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251502
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.