K260837
- 510(k) number
- K260837
- Device name
- VersaLift Expandable System
- Applicant
- Life Spine, Inc. IL · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2026-05-12
- Date received
- 2026-03-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K260837.pdf
Official FDA record: K260837
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.