Titan Spine Receives FDA Clearance on ALIF Spinal System

Spinal Tech

Titan Spine has received FDA 510(k) clearance to commercially release its Endoskeletal TAS system for anterior lumbar interbody fusion with integrated fixation screws, according to a Titan Spine news release. The system incorporates macro, micro and nano surface technology textures that are already available in its Endo TA ALIF device. It also includes three integrated grit-blasted screws that allow 10 degrees of medial/lateral or anterior/posterior angulation.

Related Articles on Spine Devices:

Spine Device Company Uses Zwick Fatigue to Test Spinal Implants

Captiva Spine Receives FDA Clearance for Pedicle Screw System

Spine Device Company Intrinsic Therapeutics Names Cary Hagan President & CEO



Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers