HOFFMAN ESTATES, Illinois — Orthopedic device maker Life Spine Inc. won 510(k) clearance from the Food & Drug Administration for two spinal systems.
Each of the systems uses what the company calls a “zero-step locking mechanism” and features designed to reduce the steps and complexity of surgical procedures, according to a press release.
The first product, the company’s Dyna-Link system, features a titanium-polymer device that allows for the use of fixed- or variable-angle screws. The second product, called the Presidio, is a spinal plating system made of titanium.
Last year, Life Spine won 510(k) clearance for what it said was the first of several minimally invasive spinal systems it plans to bring to market.
