K250186
- 510(k) number
- K250186
- Device name
- GoLIF! Lumbar Interbody Fusion System
- Applicant
- Getset Surgical, SA CH
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2025-03-21
- Date received
- 2025-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K250186.pdf
Official FDA record: K250186
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.