K-number	K161782
Device name	Arthrex Univers Revers Shoulder Prosthesis System
Applicant	Arthrex, Inc.
Product code	HSD
Device class	Class II
Decision date	Nov 21, 2016
Decision	Substantially Equivalent
Regulation	888.3690

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View the full FDA submission: accessdata.fda.gov

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Arthrex Univers Revers Shoulder Prosthesis System

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