K-number	K202192
Device name	STRUXXURE®-L and STRUXXURE®-A Plate System
Applicant	Nexxt Spine, LLC
Product code	KWQ
Device class	Class II
Decision date	Sep 17, 2020
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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STRUXXURE®-L and STRUXXURE®-A Plate System

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