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Regulatory Briefs: What's New From FDA

Medtronic gets February panel date for its DIAM spine device, which would be the firm's second interspinous spacer on the market; FDA moves risk classifications forward for five device types; and the agency continues its scrutiny of direct-to-consumer genetic tests.

FDA’s Orthopaedic and Rehabilitation Devices Panel is set to discuss Medtronic PLC's PMA for the DIAM spinal stabilization system on Feb. 19, 2016, the agency announced

in a Nov. 23 Federal Register notice.

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