K-number	K151312
Device name	VerteLP Interbody Fusion Device
Applicant	Vgi, LLC
Product code	OVD
Device class	Class II
Decision date	Jan 13, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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VerteLP Interbody Fusion Device

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