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FDA 510(k)

Arthrex Spine Compression FT Screw

K-Number: K250920 · 2025-05-22

ApplicantArthrex, Inc.
Decision Date2025-05-22
Product CodeMRW
DecisionSubstantially Equivalent

Device Summary

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 2025-05-22 under 510(k) number K250920. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex Spine Compression FT Screw?

Arthrex Spine Compression FT Screw is a medical device that received FDA 510(k) clearance on 2025-05-22. The listed applicant is Arthrex, Inc.. The 510(k) number is K250920.

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

Arthrex Spine Compression FT Screw received FDA 510(k) clearance on 2025-05-22, under 510(k) number K250920.

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.

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.

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Related Devices (Code: MRW)

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.

K261209Ion-LSurGenTec, LLCK253676CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)Providence Medical Technology, Inc.K253432DiversiVy™ Facet Screw SystemVy Spine, LLCK251714Ion-CSurGenTec, LLCK250679FFX Facet Fixation SystemSc MedicaK253190CORUS-LX ImplantProvidence Medical Technology, Inc.

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.

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