K-number	K170564
Device name	MyndMove System, MyndMove Functional Electrical Stimulator
Applicant	Myndtec, Inc.
Product code	GZI
Device class	Class II
Decision date	Aug 30, 2017
Decision	Substantially Equivalent
Regulation	882.5810

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View the full FDA submission: accessdata.fda.gov

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MyndMove System, MyndMove Functional Electrical Stimulator

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