K-number	K090714
Device name	VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM
Applicant	Medtronic Sofamor Danek
Product code	KWP
Device class	Class II
Decision date	Apr 17, 2009
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM

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