人工關節，髋關節，半限制性，金屬/金屬，表面修復
PMA 核准號：P040033 · 2025-01-10
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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 Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2025-01-10. 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 2025-01-10. The listed applicant is Smith & Nephew, Inc..
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?
FDA 510(k) 記錄將史密斯與內夫公司（Smith & Nephew, Inc.）列為申請人。這並不單獨確立設備製造商的身份。
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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