K-number	K112899
Device name	ARTHREX BIO-SUTURE
Applicant	Arthrex, Inc.
Product code	GAT
Device class	Class II
Decision date	Apr 6, 2012
Decision	Substantially Equivalent
Regulation	878.5000

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View the full FDA submission: accessdata.fda.gov

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ARTHREX BIO-SUTURE

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