FDA 510(k)

FiberTape Button

K-Number: K260405 · 2026-03-09

Decision Date2026-03-09

Product CodeMBI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

FiberTape Button is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2026-03-09 under approval number K260405. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FiberTape Button?

FiberTape Button is a medical device that received FDA 510(k) clearance on 2026-03-09. It is manufactured by Arthrex, Inc.. The 510(k) number is K260405.

When was FiberTape Button approved by the FDA?

FiberTape Button received FDA 510(k) clearance on 2026-03-09, under approval number K260405.

What company makes FiberTape Button?

FiberTape Button is manufactured by Arthrex, Inc..

What is the FDA product code for FiberTape Button?

The FDA product code for FiberTape Button is MBI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.