K-number	K001945
Device name	SYNTHES (USA) MEDIAL DISTAL TIBIA PLATES
Applicant	Synthes (Usa)
Product code	HRS
Device class	Class II
Decision date	Sep 22, 2000
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) MEDIAL DISTAL TIBIA PLATES

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