K-number	K170771
Device name	VariAx 2 Foot System
Applicant	Stryker GmbH
Product code	HRS
Device class	Class II
Decision date	May 8, 2017
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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VariAx 2 Foot System

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