K-number	K182650
Device name	Arzzt Distal Radius and Ulna System
Applicant	Truemed Group, LLC
Product code	HRS
Device class	Class II
Decision date	Jun 10, 2019
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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Arzzt Distal Radius and Ulna System

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