FDA 510(k)

Arthrex FiberTak Suture Anchor

K号: K260561 · 2026-03-20

决定日期2026-03-20

产品代码MBI

咨询委员会OR

决定Substantially Equivalent

器械摘要

Arthrex 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 2026-03-20 under 510(k) number K260561. 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 FiberTak Suture Anchor?

Arthrex FiberTak Suture Anchor is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Arthrex, Inc.. The 510(k) number is K260561.

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

Arthrex FiberTak Suture Anchor received FDA 510(k) clearance on 2026-03-20, under 510(k) number K260561.

Who is the listed applicant for Arthrex 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 FiberTak Suture Anchor?

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

列明Arthrex, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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