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Vertiflex (Tm), Incorporated

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K070218 VERTIFLEX OCTANE PEEK VERTEBRAL BODY REPLACEMENT (PEEK VBR)MQP2007-04-06 View
510(k) K062670 VERTIFLEX SPINAL SCREW SYSTEMMNH2007-01-12 View
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