K-number	K173885
Device name	Genesys Spine Binary Lumbar Plate System
Applicant	Genesys Spine
Product code	KWQ
Device class	Class II
Decision date	Apr 3, 2018
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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Genesys Spine Binary Lumbar Plate System

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