內顱內動脈瘤血流導向器
PMA 核准號：P170024 · 2026-08-28
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決定日期2026-08-28
PMA 編號P170024
產品代碼OUT
器械分類3 類
醫療專科U
諮詢委員會NE
(請提供完整的英文描述，以便進行翻譯。)
器材摘要
Intracranial aneurysm flow diverter is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2026-08-28. The device is classified under product code OUT. It was reviewed by the NE advisory panel.
常見問題
What is the Intracranial aneurysm flow diverter?
Intracranial aneurysm flow diverter is a medical device that received FDA 510(k) clearance on 2026-08-28. The listed applicant is Stryker Neurovascular.
When did Intracranial aneurysm flow diverter receive FDA 510(k) clearance?
The clearance date for Intracranial aneurysm flow diverter can be found in the official FDA records.
誰是Intracranial aneurysm flow diverter的登記申請人？
The FDA 510(k) record lists Stryker Neurovascular as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？Intracranial aneurysm flow diverter？
FDA產品代碼對於內顱動脈瘤血流導向器的為 OUT。
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。
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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