K-number	K041601
Device name	SURFIX KNEE OSTEOTOMY SYSTEM
Applicant	Surfix Technologies
Product code	HRS
Device class	Class II
Decision date	Aug 27, 2004
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SURFIX KNEE OSTEOTOMY SYSTEM

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