Life Spine Gains FDA Clearance of Steerable PLATEAU Ti Interbody

By Julie A. Vetalice

Life Spine Gains FDA Clearance of Steerable PLATEAU Ti Interbody

Life Spine received FDA 510(k) clearance to market the Steerable PLATEAU® Ti System.

Steerable PLATEAU allows controlled delivery upon insertion to facilitate positioning in the anterior portion of the disc space and features a curved design to match patient anatomy and maximize endplate coverage. The spacer was designed to restore patient sagittal balance with lordotic options of 7° and 12°.

Steerable PLATEAU Ti is available in lengths of 28mm and 32mm and heights ranging from 9mm to 14mm in 1mm increments. It features Life Spine’s proprietary OSSEO-LOC™ Surface architecture of 400 to 600 micron porosity, and is complemented by the company's CENTRIC®-T Pedicle-Based Retractor and AVATAR® MIS Spinal Fixation.

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory