K-number	K062670
Device name	VERTIFLEX SPINAL SCREW SYSTEM
Applicant	Vertiflex (Tm), Incorporated
Product code	MNH
Device class	Class II
Decision date	Jan 12, 2007
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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VERTIFLEX SPINAL SCREW SYSTEM

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