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FDA 510(k) K152568, C-VBR, by Cardinal Spine, LLC

FDA 510(k) K152568, C-VBR, by Cardinal Spine, LLC

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510(K) Number: K152568
Device Name: C-VBR
Manufacturer: Cardinal Spine, LLC
Device Classification Name: spinal vertebral body replacement device - cervical
Regulation Number: 888.3060
Classification Product Code: PLR
Date Received: 09/09/2015
Decision Date: 02/11/2016
Regulation Medical Specialty: Orthopedic
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