K-number	K011978
Device name	SYNTHES LCP PROXIMAL TIBIA PLATE
Applicant	Synthes (Usa)
Product code	HRS
Device class	Class II
Decision date	Aug 9, 2001
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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SYNTHES LCP PROXIMAL TIBIA PLATE

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