K-number	K102443
Device name	INTRAFIX TIBIAL SHEATH
Applicant	Depuy Mitek, A Johnson & Johnson Company
Product code	MBI
Device class	Class II
Decision date	Oct 20, 2010
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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INTRAFIX TIBIAL SHEATH

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