510(k) K250186 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
GoLIF! Lumbar Interbody Fusion System
| Applicant | Getset Surgical, SA, Vaud, CH |
| Decision | Substantially Equivalent, Mar 21, 2025 |
| Received | Jan 22, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250186
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.