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Home » FDA Gives Life Spine Clearance for Plateau-Lo
FDA Gives Life Spine Clearance for Plateau-Lo
![ClearanceStamp_Blue.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Blue.gif?t=1576043968&width=430)
March 21, 2018
Illinois-based Life Spine received 510(k) clearance for its Plateau-Lo insert and rotate spacer system, used for micro-invasive lumbar interbody fusions.
The product is an addition to the company’s interbody platform, combining with the company’s AVATAR percutaneous screw system and its CENTRIC-T pedicle-based retractor system for use in micro-invasive procedures.
Plateau-Lo features an aggressive tooth pattern that prevents graft migration, a bullet tip for simple insertion, and large, open graft windows to contain bone grafts and maximize visibility.
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