K-number	K080341
Device name	ENDODRAPE(TM)
Applicant	Vortek Surgical, LLC
Product code	KKX
Device class	Class II
Decision date	Jul 21, 2008
Decision	Substantially Equivalent
Regulation	878.4370

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Source

View the full FDA submission: accessdata.fda.gov

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ENDODRAPE(TM)

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