立體定位導引外科設備，NaoTrac S
K 號：K242575 · 2025-05-23
廣告
器材摘要
Stereotaxic Guiding Surgical Devices, NaoTrac S is the device name listed in this FDA 510(k) record. The listed applicant is Brain Navi Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K242575. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Stereotaxic Guiding Surgical Devices, NaoTrac S?
Stereotaxic Guiding Surgical Devices, NaoTrac S is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Brain Navi Biotechnology Co., Ltd.. The 510(k) number is K242575.
When did Stereotaxic Guiding Surgical Devices, NaoTrac S receive FDA 510(k) clearance?
Stereotaxic Guiding Surgical Devices, NaoTrac S received FDA 510(k) clearance on 2025-05-23, under 510(k) number K242575.
Who is the listed applicant for Stereotaxic Guiding Surgical Devices, NaoTrac S?
The FDA 510(k) record lists Brain Navi Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stereotaxic Guiding Surgical Devices, NaoTrac S?
The FDA product code for Stereotaxic Guiding Surgical Devices, NaoTrac S is HAW.
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：HAW）
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。
廣告