K-number	K983056
Device name	INNOVASIVE TIBIAL FASTENER
Applicant	Innovasive Devices, Inc.
Product code	MBI
Device class	Class II
Decision date	Oct 13, 1998
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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INNOVASIVE TIBIAL FASTENER

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