K-number	K170780
Device name	ARIX Foot System (2.3/2.8)
Applicant	Jeil Medical Corporation
Product code	HRS
Device class	Class II
Decision date	Aug 14, 2017
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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ARIX Foot System (2.3/2.8)

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