Life Spine Gains FDA Clearance for Additions to ARx

Life Spine was granted FDA 510(k) clearance to market implant and instrument additions to the ARx Spinal System. ARx received its original clearance in 2006; this is the system's fourth clearance update.

ARx is Life Spine's fourth 510(k) clearance in 2020, marking 92 clearances for the company overall. ARx is complemented by the PROLIFT®...

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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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