K-number	K021380
Device name	OSS LES PROXIMAL FEMORAL COMPONENT
Applicant	Biomet, Inc.
Product code	JDI
Device class	Class II
Decision date	May 28, 2002
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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OSS LES PROXIMAL FEMORAL COMPONENT

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