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Vertiflex, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K122509 VERTIFLEX SPINOUS PROCESS FIXATION PLATEKWP2012-12-17 View
510(k) K122662 VERTIFLEX DIRECT DECOMPRESSION SYSTEMHRX2012-11-13 View
510(k) K082270 OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEMMAX2008-09-16 View
510(k) K073143 MODIFIED VERTIFLEX SPINAL SCREW SYSTEMMNI2008-04-07 View
510(k) K073245 EXTENDED VERTIFLEX SPINAL SCREW SYSTEMNKB2008-02-15 View
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