K-number	K941285
Device name	ARTHREX GRAFT HARVESTING KIT
Applicant	Arthrex, Inc.
Product code	KIJ
Device class	Class I
Decision date	Nov 14, 1994
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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ARTHREX GRAFT HARVESTING KIT

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