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# FDA Clears Life Spine’s Cervical Spacer
- URL: https://www.fdaweb.com/fda-clears-life-spines-cervical-spacer/
- Published: 2016-09-20T12:00:00.000Z
- Updated: 2026-09-14T21:33:29.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5136863

FDA has cleared a Life Spine 510(k) for the PRO-LINK Ti Stand-Alone Cervical Spacer System, a stand-alone cervical interbody that is made using the company’s Osseo-Loc technology. Osseo-Loc is a proprietary surface treatment for titanium with 500-600 microns of porosity, which is intended to help create an environment for potential bone growth, the company says. “Due to the structural integrity of titanium, we were also able to include lateral graft windows for maximum bone graft volume and visibility,” it says.