K-number	K083779
Device name	MAK OSS KNEE FEMORAL COMPONENTS
Applicant	Biomet Manufacturing Corp
Product code	KRO
Device class	Class II
Decision date	Apr 3, 2009
Decision	Substantially Equivalent
Regulation	888.3510

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View the full FDA submission: accessdata.fda.gov

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MAK OSS KNEE FEMORAL COMPONENTS

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