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Spinal Tech

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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.

Despite a challenging healthcare atmosphere, the demand for new medical innovation is growing and the medical device market is expected to grow significantly over the next three years, according to a Manufacturing Group report.

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