刺激器，電氣，植入式，針對尿失禁
PMA 核准號：P240011 · 2026-09-14
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器材摘要
Stimulator, tibial, electrical, implantable, for urinary incontinence is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Neuromodulation. It received FDA 510(k) clearance on 2026-09-14. The device is classified under product code QPT. It was reviewed by the GU advisory panel.
常見問題
What is the Stimulator, tibial, electrical, implantable, for urinary incontinence?
Stimulator, tibial, electrical, implantable, for urinary incontinence is a medical device that received FDA 510(k) clearance on 2026-09-14. The listed applicant is Medtronic Neuromodulation.
When did Stimulator, tibial, electrical, implantable, for urinary incontinence receive FDA 510(k) clearance?
The clearance date for Stimulator, tibial, electrical, implantable, for urinary incontinence can be found in the official FDA records.
誰是電氣植入式膝蓋刺激器，用於尿失禁的登記申請人？
The FDA 510(k) record lists Medtronic Neuromodulation as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為何？針對電氣植入式膝蓋刺激器，用於尿失禁？
FDA產品代碼為電氣植入式膝蓋刺激器，用於尿失禁治療的是QPT。
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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