K-number	K200523
Device name	Biolign® Roto-Loc Cervical Plate System
Applicant	Elite Surgical Supplies (Pty), Ltd.
Product code	KWQ
Device class	Class II
Decision date	Apr 30, 2020
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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Biolign® Roto-Loc Cervical Plate System

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