K-number	K182039
Device name	Arthrex Univers Revers Porous Coated Baseplate and Universal Glenoid Inlay
Applicant	Arthrex, Inc.
Product code	PHX
Device class	Class II
Decision date	Sep 28, 2018
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 Porous Coated Baseplate and Universal Glenoid Inlay

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