K-number	K141635
Device name	ARTHREX IBALANCE TKA SYSTEM
Applicant	Arthrex, Inc.
Product code	MBH
Device class	Class II
Decision date	Sep 3, 2014
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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ARTHREX IBALANCE TKA SYSTEM

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