K-number	K223853
Device name	Medartis APTUS® Ulna Plates
Applicant	Medartis AG
Product code	HRS
Device class	Class II
Decision date	Mar 30, 2023
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Medartis APTUS® Ulna Plates

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