Class Class II

Arthrex SutureTak Suture Anchor (K252314)

K252314 2025-10-29 Traditional
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Description

Arthrex SutureTak Suture Anchor by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252314
Clearance Date2025-10-29
Clearance TypeTraditional
Product CodeMBI
Regulation Number888.3040

Categories

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