人工義肢，踝部，非粘合，非限制
PMA 核准號：P160036 · 2026-07-31
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器材摘要
Prosthesis, ankle, uncemented, non-constrained is the device name listed in this FDA 510(k) record. The listed applicant is Dt Medtech, LLC. It received FDA 510(k) clearance on 2026-07-31. The device is classified under product code NTG. It was reviewed by the OR advisory panel.
常見問題
What is the Prosthesis, ankle, uncemented, non-constrained?
Prosthesis, ankle, uncemented, non-constrained is a medical device that received FDA 510(k) clearance on 2026-07-31. The listed applicant is Dt Medtech, LLC.
When did Prosthesis, ankle, uncemented, non-constrained receive FDA 510(k) clearance?
The clearance date for Prosthesis, ankle, uncemented, non-constrained can be found in the official FDA records.
誰是Prosthesis, ankle, uncemented, non-constrained的登記申請人？
The FDA 510(k) record lists Dt Medtech, LLC as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為Prosthesis, ankle, uncemented, non-constrained的是什麼？
FDA產品代碼對於人工足踝，非粘合，非限制性的是NTG。
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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