K-number	K061385
Device name	OSSTAPLE, OSSPLATE, OSSFORCE
Applicant	Biomedical Enterprises, Inc.
Product code	KWQ
Device class	Class II
Decision date	May 30, 2007
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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OSSTAPLE, OSSPLATE, OSSFORCE

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