www.fdanews.com/articles/175671-life-spine-receives-fda-clearance-for-prolift-expandable-interbody-system
Life Spine Receives FDA Clearance for PROLIFT Expandable Interbody System
March 9, 2016
The FDA has granted 510(k) clearance to Life Spine for its PROLIFT Expandable Interbody System.
The device is a minimally invasive solution, designed for surgical treatment of spinal disorders, and is intended for use with a midline thoracolumbar screw system.
“Once implanted, it can expand cephalad to caudal to accommodate disc height ranges from 8mm to 16mm for varying patient anatomy,” according to Rich Mueller, COO.
A limited release is expected during the second quarter, with a full product release later in the year, the company says. — Anisa Jibrell