K-number	K231113
Device name	Arthrex FiberTak Suture Anchor
Applicant	Arthrex, Inc.
Product code	MBI
Device class	Class II
Decision date	May 18, 2023
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Arthrex FiberTak Suture Anchor

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