K-number	K160051
Device name	NuVasive® Interfixated Interbody System
Applicant	Nu Vasive, Incorporated
Product code	OVD
Device class	Class II
Decision date	Apr 20, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive® Interfixated Interbody System

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