K-number	K050669
Device name	JEIL BONE FIXATION SYSTEM
Applicant	Jeil Medical Corporation
Product code	JEY
Device class	Class II
Decision date	May 26, 2005
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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JEIL BONE FIXATION SYSTEM

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