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Vertiflex Superion Spacer Panel Reset To Give FDA More Review Time

FDA's Orthopaedics and Rehabilitation Devices Panel had planned to consider Vertiflex's PMA for its Superion interspinous spacer device on Dec. 12, but the agency postponed the meeting to Feb. 20 give it more time to review device information.

An FDA advisory panel meeting on VertiFlex Inc.’s Superion interspinous spacer device that was scheduled for Dec. 12 has been postponed until Feb. 20 “due to the FDA needing additional time to review information which had been supplied by the sponsor,” according to an agency spokeswoman.

Superion is a motion-preserving, indirect-compression spinal implant system intended to treat patients suffering symptoms and

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