K-number	K190227
Device name	Boomerang Anterior Cervical Plate System
Applicant	Choicespine, LP
Product code	KWQ
Device class	Class II
Decision date	May 1, 2019
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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Boomerang Anterior Cervical Plate System

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Boomerang Anterior Cervical Plate System