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# Life Spine Prolift Lateral Expandable Spacer Cleared
- URL: https://www.fdaweb.com/life-spine-prolift-lateral-expandable-spacer-cleared/
- Published: 2019-06-18T12:00:00.000Z
- Updated: 2026-09-15T01:33:26.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5144363

FDA has cleared a Life Spine 510(k) for the Prolift Lateral Expandable Spacer System for use in treating spinal disorders. The device, which is available in several lordotic options, allows for post-packing *in situ*, has anatomically convex endplates and is made using Life Spine’s proprietary Osseo-Loc surface technology, the company says. It also features minimal insertion height and controlled, *in situ* expansion for lateral interbody fusion procedures.