FDA 510(k)

Arthrex Spine Compression FT Screw

K号: K262618 · 2026-09-24

决定日期2026-09-24

产品代码MRW

决定Substantially Equivalent

器械摘要

Arthrex Spine Compression FT Screw is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2026-09-24 under 510(k) number K262618. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

常见问题

What is the Arthrex Spine Compression FT Screw?

Arthrex Spine Compression FT Screw is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Arthrex, Inc.. The 510(k) number is K262618.

When did Arthrex Spine Compression FT Screw receive FDA 510(k) clearance?

Arthrex Spine Compression FT Screw received FDA 510(k) clearance on 2026-09-24, under 510(k) number K262618.

Who is the listed applicant for Arthrex Spine Compression FT Screw?

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 Spine Compression FT Screw?

The FDA product code for Arthrex Spine Compression FT Screw is MRW.

列明Arthrex, Inc.为申报人的其他记录

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