K-number	K011007
Device name	TENODESIS SCREW, 5.5 MM, MODEL AR-1350-55
Applicant	Arthrex, Inc.
Product code	MBI
Device class	Class II
Decision date	Jun 12, 2001
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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TENODESIS SCREW, 5.5 MM, MODEL AR-1350-55

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