針對股動脈表層的支架
PMA 核准號：P160025 · 2026-09-11
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器材摘要
STENT, SUPERFICIAL FEMORAL ARTERY is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik AG. It received FDA 510(k) clearance on 2026-09-11. The device is classified under product code NIP. It was reviewed by the CV advisory panel.
常見問題
What is the STENT, SUPERFICIAL FEMORAL ARTERY?
STENT, SUPERFICIAL FEMORAL ARTERY is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Biotronik AG.
When did STENT, SUPERFICIAL FEMORAL ARTERY receive FDA 510(k) clearance?
The clearance date for STENT, SUPERFICIAL FEMORAL ARTERY can be found in the official FDA records.
誰是STENT, SUPERFICIAL FEMORAL ARTERY的列名申請人？
The FDA 510(k) record lists Biotronik AG as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為STENT, SUPERFICIAL FEMORAL ARTERY是什麼？
FDA產品代碼對於STENT, SUPERFICIAL FEMORAL ARTERY為NIP。
相關臨床試驗
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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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