K-number	K100676
Device name	SYNTHES TOMOFIX(TM) MEIAL HIGH TIBIA PLATE, SMALL
Applicant	Synthes (Usa)
Product code	HRS
Device class	Class II
Decision date	Apr 8, 2010
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SYNTHES TOMOFIX(TM) MEIAL HIGH TIBIA PLATE, SMALL

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