內顱腔輔助支架
PMA 核准號：P170013 · 2026-09-16
廣告
決定日期2026-09-16
PMA 編號P170013
產品代碼QCA
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 coil-assist stent is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code QCA. It was reviewed by the NE advisory panel.
常見問題
What is the Intracranial coil-assist stent?
Intracranial coil-assist stent is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is MicroVention, Inc..
When did Intracranial coil-assist stent receive FDA 510(k) clearance?
The clearance date for Intracranial coil-assist stent can be found in the official FDA records.
Who is the listed applicant for Intracranial coil-assist stent?
The FDA 510(k) record lists MicroVention, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intracranial coil-assist stent?
The FDA product code for Intracranial coil-assist stent is QCA.
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。
廣告