K-number	K091679
Device name	LEFORTE SYSTEM BONE PLATE
Applicant	Jeil Medical Corporation
Product code	JEY
Device class	Class II
Decision date	Oct 2, 2009
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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LEFORTE SYSTEM BONE PLATE

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