K-number	K170675
Device name	Graftgun Universal Graft Delivery System
Applicant	SurGenTec, LLC
Product code	FMF
Device class	Class II
Decision date	Jul 19, 2017
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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Graftgun Universal Graft Delivery System

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