Life Spine Receives FDA Clearance for PROLIFT Expandable Interbody System
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