K-number	K212415
Device name	Arthrex Modular Glenoid System-Titanium Glenosphere
Applicant	Arthrex, Inc.
Product code	PHX
Device class	Class II
Decision date	Nov 17, 2021
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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Arthrex Modular Glenoid System-Titanium Glenosphere

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