Atlas Spine Gains 510(k) for HiJAK Expandable LLIF

Atlas Spine Announces FDA Clearance of its HiJAK Expandable Lateral Lumbar Interbody Fusion System

Atlas Spine was granted FDA 510(k) clearance to market the HiJAK Expandable Lateral Lumbar Interbody System.

Designed with both integrated fixation and without, and options which gain up to 30 degrees of angulation, the system provides surgeons the opportunity to adjust the implant intra-operatively, to “tailor fit” each patient’s specific...

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JV

Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.



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