K-number	K160003
Device name	Sniper (R) Spine System
Applicant	Spine Wave, Inc.
Product code	MNI
Device class	Class II
Decision date	Feb 26, 2016
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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Sniper (R) Spine System

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