K-number	K191960
Device name	Arthrex Univers Revers Modular Glenoid System
Applicant	Arthrex, Inc.
Product code	PHX
Device class	Class II
Decision date	Dec 23, 2019
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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Arthrex Univers Revers Modular Glenoid System

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