GoLIF! Lumbar Interbody Fusion System is an AI-enabled medical device from GetSet Surgical, SA that the U.S. FDA cleared through 510(k) K250186 on March 21, 2025. Its lead review panel is Orthopedic and its primary product code is MAX (Intervertebral Fusion Device With Bone Graft, Lumbar).
See also all FDA AI clearances in 2025.
Key facts
| Submission number | K250186 |
|---|---|
| Pathway | 510(k) |
| Date of final decision | |
| Company (FDA list) | GetSet Surgical, SA |
| Lead review panel | Orthopedic |
| Primary product code | MAX — Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant (openFDA) | Getset Surgical, SA |
| Applicant location | Vaud, CH |
| Device class | Class 2 |
| Regulation number | 21 CFR 888.3080 |
| Decision code | SESE |
| Submission type | Traditional |
Source: FDA AI-Enabled Medical Devices list and openFDA.
What this means
A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. GoLIF! Lumbar Interbody Fusion System went through this pathway (K250186).
openFDA lists it as a Class 2 device under 21 CFR 888.3080. Class II devices are moderate risk and are subject to general and special controls.
Product code MAX covers 1 device on the FDA AI list. By decision date, this device is #1 of 1 under that code. GetSet Surgical, SA has 1 AI-enabled device on the list, and the Orthopedic panel accounts for 8 in total.
Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.