Arthrex 腰椎壓縮 FT 螺釘
K 號：K262618 · 2026-09-24
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器材摘要
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.
常見問題
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.
相關臨床試驗
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其他以 Arthrex, Inc. 為申請人之記錄
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
相關器械（代碼：MRW）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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.
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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