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Author: Staff

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VertiFlex announced that the U.S. Food and Drug Administration has scheduled an Orthopedic and Rehabilitation Devices Advisory Panel meeting on Feb. 20, 2015 to discuss and vote on its premarket approval application for the Superion Interspinous Spacer System.

The Spine Journal published a report recently comparing the results from the SPORT lumbar disc herniation cohort with the National Surgical Quality Improvement Program database to identify different trends in disc herniation treatment. 

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