K-number	K141812
Device name	MYGAIT STIMULATION SYSTEM
Applicant	Otto Bock Healthcare Products GmbH
Product code	GZI
Device class	Class II
Decision date	Apr 2, 2015
Decision	Substantially Equivalent
Regulation	882.5810

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Source

View the full FDA submission: accessdata.fda.gov

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MYGAIT STIMULATION SYSTEM

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