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# FDA Clears Life Spine Lumbar Spacer
- URL: https://www.fdaweb.com/fda-clears-life-spine-lumbar-spacer/
- Published: 2020-08-11T12:00:00.000Z
- Updated: 2026-09-14T16:24:33.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147403

FDA has cleared a Life Spine 510(k) for the Plateau-X Ti Lateral Lumbar Spacer System. The device is intended for use by surgeons to provide anterior column support through a lateral approach. It includes a comprehensive set of instruments and implants to streamline the surgical procedure, the company says. The system also features Osseo-Loc Titanium Surface Treatment Technology, a convex design to maximize vertebrae endplate contact for patient fitting, and large open graft windows for maximum visibility and bone graft containment, it says.