K-number	K210050
Device name	Augmented VaultLock Glenoid
Applicant	Arthrex, Inc.
Product code	KWS
Device class	Class II
Decision date	Jun 7, 2021
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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Augmented VaultLock Glenoid

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