Orthopedics
GoLIF! Lumbar Interbody Fusion System
GetSet Surgical, SA
FDA-cleared AI medical device
Intended to stabilize spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.
FDA Submission Metadata
- Submission number
- K250186
- Decision date
- March 2025
- FDA panel
- Orthopedic
- Product code
- MAX
This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.
This entry is on our editorial review queue. Full evaluation — performance metrics, clinical evidence, safety record — lands as our review pipeline graduates each device. The information above is what's been verified to date.