FDA 510(k)

AXS Lift 颅内基底導管

K 號：K253032 · 2026-02-11

決定日期2026-02-11

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

AXS Lift Intracranial Base Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2026-02-11 under 510(k) number K253032. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AXS Lift Intracranial Base Catheter?

AXS Lift Intracranial Base Catheter is a medical device that received FDA 510(k) clearance on 2026-02-11. The listed applicant is Stryker Neurovascular. The 510(k) number is K253032.

When did AXS Lift Intracranial Base Catheter receive FDA 510(k) clearance?

AXS Lift Intracranial Base Catheter received FDA 510(k) clearance on 2026-02-11, under 510(k) number K253032.

Who is the listed applicant for AXS Lift Intracranial Base Catheter?

The FDA 510(k) record lists Stryker Neurovascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AXS Lift Intracranial Base Catheter?

The FDA product code for AXS Lift Intracranial Base Catheter is QJP.

其他以 Stryker Neurovascular 為申請人之記錄

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相關器械（代碼：QJP）

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。

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