FDA 510(k)

Arthrex Nano FiberTak Suture Anchor

K号: K254229 · 2026-03-02

决定日期2026-03-02

产品代码MBI

咨询委员会OR

决定Substantially Equivalent

器械摘要

Arthrex Nano FiberTak Suture Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2026-03-02 under 510(k) number K254229. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Arthrex Nano FiberTak Suture Anchor?

Arthrex Nano FiberTak Suture Anchor is a medical device that received FDA 510(k) clearance on 2026-03-02. The listed applicant is Arthrex, Inc.. The 510(k) number is K254229.

When did Arthrex Nano FiberTak Suture Anchor receive FDA 510(k) clearance?

Arthrex Nano FiberTak Suture Anchor received FDA 510(k) clearance on 2026-03-02, under 510(k) number K254229.

Who is the listed applicant for Arthrex Nano FiberTak Suture Anchor?

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 Arthrex Nano FiberTak Suture Anchor?

The FDA product code for Arthrex Nano FiberTak Suture Anchor is MBI.

列明Arthrex, Inc.为申报人的其他记录

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