K-number	K141232
Device name	APTUS ULNA SHORTENING 2.5
Applicant	Medartis AG
Product code	HRS
Device class	Class II
Decision date	Jun 23, 2014
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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APTUS ULNA SHORTENING 2.5

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