Trax EX 總結器
K 號：K251750 · 2026-03-12
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器材摘要
Trax EX Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Trax Surgical, Inc.. It received FDA 510(k) clearance on 2026-03-12 under 510(k) number K251750. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Trax EX Anchor?
Trax EX Anchor is a medical device that received FDA 510(k) clearance on 2026-03-12. The listed applicant is Trax Surgical, Inc.. The 510(k) number is K251750.
When did Trax EX Anchor receive FDA 510(k) clearance?
Trax EX Anchor received FDA 510(k) clearance on 2026-03-12, under 510(k) number K251750.
Who is the listed applicant for Trax EX Anchor?
The FDA 510(k) record lists Trax Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trax EX Anchor?
The FDA product code for Trax EX Anchor is MBI.
相關臨床試驗
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：MBI）
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。
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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