K-number	K914169
Device name	WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP
Applicant	Dow Corning Wright
Product code	JWH
Device class	Class II
Decision date	Jan 27, 1992
Decision	Substantially Equivalent
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP

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