K-number	K212581
Device name	VariAx 2 Distal Radius System, VariAx 2 Distal Ulna System
Applicant	Stryker GmbH
Product code	HRS
Device class	Class II
Decision date	Jan 19, 2022
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 Distal Radius System, VariAx 2 Distal Ulna System

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