人工關節，髋關節，半限制性，金屬/陶瓷/陶瓷/金屬，固定或不固定
PMA 核准號：P030027 · 2018-02-16
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器材摘要
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is the device name listed in this FDA 510(k) record. The listed applicant is Microport Orthopedics, Inc.. It received FDA 510(k) clearance on 2018-02-16. The device is classified under product code MRA. It was reviewed by the OR advisory panel.
常見問題
What is the Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented?
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is a medical device that received FDA 510(k) clearance on 2018-02-16. The listed applicant is Microport Orthopedics, Inc..
When did Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented receive FDA 510(k) clearance?
The clearance date for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented can be found in the official FDA records.
誰是Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented的登記申請人？
FDA 510(k) 記錄將 Microport Orthopedics, Inc. 列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented是什麼？
FDA產品代碼對於人工關節，半限制性，金屬/陶瓷/陶瓷/金屬，固定或不固定的是MRA。
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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