K-number	K925900
Device name	LACEY REVISION FEMORAL COMPONENT
Applicant	Dow Corning Wright
Product code	JWH
Device class	Class II
Decision date	Aug 24, 1993
Decision	Substantially Equivalent
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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LACEY REVISION FEMORAL COMPONENT

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