Vertiflex, Inc.

5 FDA 510(k) medical device clearances.

Top product codes for Vertiflex, Inc.

Recent clearances by Vertiflex, Inc.

K122509 — VERTIFLEX SPINOUS PROCESS FIXATION PLATE KWP · 2012-12-17
K122662 — VERTIFLEX DIRECT DECOMPRESSION SYSTEM HRX · 2012-11-13
K082270 — OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM MAX · 2008-09-16
K073143 — MODIFIED VERTIFLEX SPINAL SCREW SYSTEM MNI · 2008-04-07
K073245 — EXTENDED VERTIFLEX SPINAL SCREW SYSTEM NKB · 2008-02-15

Data sourced from openFDA. This site is unofficial and independent of the FDA.