Class Class II

Arthrex FiberTak Suture Anchor (K231113)

K231113 2023-05-18 Special
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Description

Arthrex FiberTak Suture Anchor by Arthrex, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK231113
Clearance Date2023-05-18
Clearance TypeSpecial
Product CodeMBI
Regulation Number888.3040

Categories

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