FDA 510(k) Applications Submitted by VERTIFLEX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K082270 08/11/2008 OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM VERTIFLEX, INC.
K122509 08/17/2012 VERTIFLEX SPINOUS PROCESS FIXATION PLATE VERTIFLEX, INC.
K122662 08/31/2012 VERTIFLEX DIRECT DECOMPRESSION SYSTEM VERTIFLEX, INC.
K073143 11/07/2007 MODIFIED VERTIFLEX SPINAL SCREW SYSTEM VERTIFLEX, INC.
K073245 11/19/2007 EXTENDED VERTIFLEX SPINAL SCREW SYSTEM VERTIFLEX, INC.


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