K-number	K252314
Device name	Arthrex SutureTak Suture Anchor
Applicant	Arthrex, Inc.
Product code	MBI
Device class	Class II
Decision date	Oct 29, 2025
Decision	Substantially Equivalent
Regulation	888.3040

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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Arthrex SutureTak Suture Anchor

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