Life Spine’s Gruve anterior cervical plate system receives 510(k) marketing clearance

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The US Food and Drug Administration (FDA) has granted 510(k) marketing clearance to Life Spine’s Gruve anterior cervical plate system.

This system is designed to allow for extreme bone screw angulation and large graft windows. According to the company, its design should also allow for tactile and visual confirmation of the locking mechanism during final screw placement.

Gruve is scheduled for limited release at the beginning of 2016 with full product release expected in the second quarter of 2016.

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