Clearance Summary
Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System received FDA 510(k) clearance under submission number K253748, sponsored by Life Spine, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2026-01-23.
- Submission: K253748
- Applicant / Sponsor: Life Spine, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2026-01-23
Classification & Regulation
This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.