K-number	K071612
Device name	MODUS TRILOCK 2.0/2.3/2.5
Applicant	Medartis AG
Product code	JEY
Device class	Class II
Decision date	Sep 11, 2007
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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MODUS TRILOCK 2.0/2.3/2.5

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