FiberTape Button
K-Number: K260405 · 2026-03-09
Device Summary
Frequently Asked Questions
What is the FiberTape Button?
FiberTape Button is a medical device that received FDA 510(k) clearance on 2026-03-09. The listed applicant is Arthrex, Inc.. The 510(k) number is K260405.
When did FiberTape Button receive FDA 510(k) clearance?
FiberTape Button received FDA 510(k) clearance on 2026-03-09, under 510(k) number K260405.
Who is the listed applicant for FiberTape Button?
The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FiberTape Button?
The FDA product code for FiberTape Button is MBI.
Other records listing Arthrex, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MBI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.