K-number	K871776
Device name	WHITESIDE ORTHOLOC II REV POST STAB TOTAL KNEE SY
Applicant	Dow Corning Wright
Product code	JWH
Device class	Class II
Decision date	Aug 3, 1987
Decision	Substantially Equivalent for Some Indications
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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WHITESIDE ORTHOLOC II REV POST STAB TOTAL KNEE SY

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