K-number	K992682
Device name	MODUS 2.5 MANDIBULAR RECONSTRUCTION SET
Applicant	Medartis AG
Product code	JEY
Device class	Class II
Decision date	Nov 24, 1999
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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MODUS 2.5 MANDIBULAR RECONSTRUCTION SET

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