K-number	K162313
Device name	NuVasive Next Generation NVM5 System
Applicant	Nu Vasive, Incorporated
Product code	PDQ
Device class	Class II
Decision date	Mar 16, 2017
Decision	Substantially Equivalent
Regulation	874.1820

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive Next Generation NVM5 System

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