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Centinel Spine Secures FDA Approval for Two-Level Use of prodiscC Vivo and prodiscC SK Devices

WEST CHESTER, PA — Centinel Spine®, LLC has received U.S. Food and Drug Administration (FDA) Premarket Approval for two-level indications of its prodiscC Vivo and prodiscC SK cervical total disc ...
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Nevro Receives FDA 510(k) Clearance to Use SI Fixation System Without Need to Include Lateral Screw

REDWOOD CITY, Calif., Feb. 28, 2024 /PRNewswire/ -- Nevro Corp. (NYSE: NVRO), a global medical device company delivering comprehensive, life-changing solutions for the treatment of chronic pain, today ...