K-number	K093319
Device name	NUVASIVE VUEPOINT OCT SYSTEM
Applicant	Nuvasive, Inc.
Product code	KWP
Device class	Class II
Decision date	Jun 23, 2010
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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NUVASIVE VUEPOINT OCT SYSTEM

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