Stealth AXiS 頭部臨床應用
K 號:K253379 · 2026-03-26
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器材摘要
常見問題
What is the Stealth AXiS Cranial clinical application?
Stealth AXiS Cranial clinical application is a medical device that received FDA 510(k) clearance on 2026-03-26. The listed applicant is Medtronic Navigation, Inc.. The 510(k) number is K253379.
When did Stealth AXiS Cranial clinical application receive FDA 510(k) clearance?
Stealth AXiS Cranial clinical application received FDA 510(k) clearance on 2026-03-26, under 510(k) number K253379.
Who is the listed applicant for Stealth AXiS Cranial clinical application?
The FDA 510(k) record lists Medtronic Navigation, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stealth AXiS Cranial clinical application?
The FDA product code for Stealth AXiS Cranial clinical application 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。
其他以 Medtronic Navigation, 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: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。
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