www.fdanews.com/articles/177236-centinel-spines-stalif-l-gains-clearance-in-australia
Centinel Spine’s STALIF L Gains Clearance in Australia
June 23, 2016
The Australian Therapeutic Goods Administration has cleared Centinel Spine’s STALIF L No-Profile, lateral lumbar integrated interbody system, the company announced Wednesday, which is intended for spinal fusion procedures.
The device provides compressive lag fixation with anti-backout technology and 12 degrees of lordosis, according to the company.
The company recently gained FDA clearance for its posterior cervical stabilization system, ALTOS PCT. — Anisa Jibrell