K-number	K983120
Device name	BICORTICAL SCREW
Applicant	Oraltronics Marketing-Und Vertriebs GmbH
Product code	DZE
Device class	Class II
Decision date	Jul 29, 1999
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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BICORTICAL SCREW

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