人工關節，髋關節，半限制性，金屬/金屬，表面修復
PMA 核准號：P050016 · 2020-07-17
廣告
器材摘要
Prosthesis, hip, semi-constrained, metal/metal, resurfacing is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2020-07-17. The device is classified under product code NXT. It was reviewed by the OR advisory panel.
常見問題
What is the Prosthesis, hip, semi-constrained, metal/metal, resurfacing?
Prosthesis, hip, semi-constrained, metal/metal, resurfacing is a medical device that received FDA 510(k) clearance on 2020-07-17. The listed applicant is Corin USA.
When did Prosthesis, hip, semi-constrained, metal/metal, resurfacing receive FDA 510(k) clearance?
The clearance date for Prosthesis, hip, semi-constrained, metal/metal, resurfacing can be found in the official FDA records.
Who is the listed applicant for Prosthesis, hip, semi-constrained, metal/metal, resurfacing?
The FDA 510(k) record lists Corin USA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prosthesis, hip, semi-constrained, metal/metal, resurfacing?
The FDA product code for Prosthesis, hip, semi-constrained, metal/metal, resurfacing is NXT.
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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