K-number	K180038
Device name	NuVasive Pulse System
Applicant	Nu Vasive, Incorporated
Product code	OLO
Device class	Class II
Decision date	Jun 29, 2018
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive Pulse System

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