刺激器，脊髓，完全植入式，用於疼痛緩解
PMA 核准號：P130028 · 2020-05-05
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決定日期2020-05-05
PMA 編號P130028
產品代碼LGW
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
Stimulator, spinal-cord, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Nuvectra Corporation. It received FDA 510(k) clearance on 2020-05-05. The device is classified under product code LGW. It was reviewed by the NE advisory panel.
常見問題
What is the Stimulator, spinal-cord, totally implanted for pain relief?
Stimulator, spinal-cord, totally implanted for pain relief is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Nuvectra Corporation.
When did Stimulator, spinal-cord, totally implanted for pain relief receive FDA 510(k) clearance?
The clearance date for Stimulator, spinal-cord, totally implanted for pain relief can be found in the official FDA records.
誰是Stimulator,脊髓植入，完全植入式疼痛緩解設備的登記申請人？
The FDA 510(k) record lists Nuvectra Corporation as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為何是針對完全植入性脊髓刺激器，用於疼痛緩解？
FDA產品代碼為Stimulator, 腰椎，完全植入式疼痛緩解設備的是LGW。
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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