K-number	K231657
Device name	AGILON® XO Shoulder Replacement System
Applicant	Implantcast GmbH
Product code	KWT
Device class	Class II
Decision date	Feb 16, 2024
Decision	Substantially Equivalent
Regulation	888.3650

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Source

View the full FDA submission: accessdata.fda.gov

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AGILON® XO Shoulder Replacement System

Everything you need for a 510(k) submission. Nothing you don't.