K-number	K150474
Device name	NuVasive VuePoint II OCT System
Applicant	Nu Vasive, Incorporated
Product code	NKG
Device class	Class II
Decision date	Oct 21, 2015
Decision	Substantially Equivalent
Regulation	888.3075

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View the full FDA submission: accessdata.fda.gov

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NuVasive VuePoint II OCT System

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