K-number	K220441
Device name	CYGNUS MoRe Anterior Cervical Plate System
Applicant	MiRus, LLC
Product code	KWQ
Device class	Class II
Decision date	Sep 16, 2022
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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CYGNUS MoRe Anterior Cervical Plate System

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CYGNUS MoRe Anterior Cervical Plate System