510(k) K243668 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ProLift Pivot Expandable Spacer System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Jan 23, 2025 |
| Received | Nov 27, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243668
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.