K-number	K073143
Device name	MODIFIED VERTIFLEX SPINAL SCREW SYSTEM
Applicant	Vertiflex, Inc.
Product code	MNI
Device class	Class II
Decision date	Apr 7, 2008
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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MODIFIED VERTIFLEX SPINAL SCREW SYSTEM

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