K-number	K162760
Device name	Spine Wave Anterior Cervical Spine System
Applicant	Spine Wave, Inc.
Product code	OVE
Device class	Class II
Decision date	Feb 16, 2017
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Spine Wave Anterior Cervical Spine System

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