K-number	K081111
Device name	LEGION HINGE KNEE SYSTEM
Applicant	Smith & Nephew, Inc.
Product code	KRO
Device class	Class II
Decision date	Jul 23, 2008
Decision	Substantially Equivalent
Regulation	888.3510

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View the full FDA submission: accessdata.fda.gov

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LEGION HINGE KNEE SYSTEM

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