K-number	K111397
Device name	TITAN TI SUTURE ANCHOR SYSTEM
Applicant	Arthrocare Corp.
Product code	MBI
Device class	Class II
Decision date	Jul 12, 2011
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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TITAN TI SUTURE ANCHOR SYSTEM

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