K-number	K023488
Device name	OSSTAPLE, CRANIOFACIAL
Applicant	Biomedical Enterprises, Inc.
Product code	JEY
Device class	Class II
Decision date	Oct 31, 2002
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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OSSTAPLE, CRANIOFACIAL

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