Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact