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FDA 510(k) Applications Submitted by VERTIFLEX (TM), INCORPORATED
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070218
01/23/2007
VERTIFLEX OCTANE PEEK VERTEBRAL BODY REPLACEMENT (PEEK VBR)
VERTIFLEX (TM), INCORPORATED
K062670
09/07/2006
VERTIFLEX SPINAL SCREW SYSTEM
VERTIFLEX (TM), INCORPORATED
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