K-number	K033767
Device name	DUAL TOP ANCHOR SYSTEM SCREWS
Applicant	Jeil Medical Corporation
Product code	DZE
Device class	Class II
Decision date	Feb 24, 2004
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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DUAL TOP ANCHOR SYSTEM SCREWS

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