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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 a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2025-05-22 under approval 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. It is manufactured by Arthrex, Inc.. The 510(k) number is K250920.

When was Arthrex Spine Compression FT Screw approved by the FDA?

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

What company makes Arthrex Spine Compression FT Screw?

Arthrex Spine Compression FT Screw is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Spine Compression FT Screw?

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

Related Clinical Trials

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Related Devices (Code: MRW)

K161798FacetBRIDGE® SystemLdr Spine USA, Inc. K152137FacetBRIDGE SystemLdr Spine USA K163374ALLY™ Facet ScrewsProvidence Medical Technology, Inc. K180729FaSet Fixation SystemHuvexel Co. , Ltd. K173198Facet Screw Fixation SystemU&I Corporation K192744CORRIDOR Fixation SystemGlobus Medical, 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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