Vertiflex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VERTIFLEX SPINOUS PROCESS FIXATION PLATE, VERTIFLEX DIRECT DECOMPRESSION SYSTEM, OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vertiflex, Inc. Orthopedic ✕
5 devices
Cleared
Dec 17, 2012
VERTIFLEX SPINOUS PROCESS FIXATION PLATE
Orthopedic
122d
Cleared
Nov 13, 2012
VERTIFLEX DIRECT DECOMPRESSION SYSTEM
Orthopedic
74d
Cleared
Sep 16, 2008
OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM
Orthopedic
36d
Cleared
Apr 07, 2008
MODIFIED VERTIFLEX SPINAL SCREW SYSTEM
Orthopedic
152d
Cleared
Feb 15, 2008
EXTENDED VERTIFLEX SPINAL SCREW SYSTEM
Orthopedic
88d