K-number	K180198
Device name	NuVasive® VuePoint® II OCT System
Applicant	Nu Vasive, Incorporated
Product code	NKG
Device class	Class II
Decision date	Mar 15, 2018
Decision	Substantially Equivalent
Regulation	888.3075

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive® VuePoint® II OCT System

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