Life Spine receives US FDA 510(k) clearance for Steerable Plateau Ti system

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Life Spine has announced that it has received 510(k) clearance from the US Food & Drug Administration (FDA) to market the Steerable Plateau Ti system.

The Steerable Plateau Ti System is available in lengths of 28mm and 32mm and heights ranging from 9mm–14mm in 1mm increments. The system features Life Spine’s proprietary Osseo-Loc surface architecture of 400–600 micron porosity. The Steerable Plateau Ti system is complemented by Life Spine’s Centric-T pedicle-based retractor system and the Avatar MIS spinal fixation system, the company said in a press release.

“The Steerable Plateau Ti system is one of many novel systems slated to join our Micro Invasive portfolio this year,” said Michael Butler, president and CEO of Life Spine. “These launches are testimony to our continued dedication in supporting less invasive procedures. The Steerable PLATEAU Ti system allows for 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. Additionally, the spacer was designed to restore patient sagittal balance with lordotic options of 7 degrees and 12 degrees.”


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