應用式骨科全膝關節置換系統
K 號：K163585 · 2017-06-02
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器材摘要
Responsive Orthopedics Total Hip Arthroplasty System is the device name listed in this FDA 510(k) record. The listed applicant is Responsive Orthopedics, LLC. It received FDA 510(k) clearance on 2017-06-02 under 510(k) number K163585. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Responsive Orthopedics Total Hip Arthroplasty System?
Responsive Orthopedics Total Hip Arthroplasty System is a medical device that received FDA 510(k) clearance on 2017-06-02. The listed applicant is Responsive Orthopedics, LLC. The 510(k) number is K163585.
When did Responsive Orthopedics Total Hip Arthroplasty System receive FDA 510(k) clearance?
Responsive Orthopedics Total Hip Arthroplasty System received FDA 510(k) clearance on 2017-06-02, under 510(k) number K163585.
Who is the listed applicant for Responsive Orthopedics Total Hip Arthroplasty System?
The FDA 510(k) record lists Responsive Orthopedics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Responsive Orthopedics Total Hip Arthroplasty System?
The FDA product code for Responsive Orthopedics Total Hip Arthroplasty System is LZO.
相關臨床試驗
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相關器械（代碼：LZO）
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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