刺激器，神經末梢，完全植入式，用於下肢截肢後慢性難治性疼痛
PMA 核准號：P230020 · 2026-05-05
廣告
器材摘要
常見問題
What is the stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb?
stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb is a medical device that received FDA 510(k) clearance on 2026-05-05. The listed applicant is Neuros Medical, Inc..
When did stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb receive FDA 510(k) clearance?
The clearance date for stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb can be found in the official FDA records.
Who is the listed applicant for stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb?
The FDA 510(k) record lists Neuros Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb?
The FDA product code for stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb is SAZ.
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