CPM醫療顧問公司 髌骨修復膝關節系統
K 號:K210695 · 2021-08-16
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器材摘要
常見問題
What is the CPM Medical Consultants Tibial Revision Knee System?
CPM Medical Consultants Tibial Revision Knee System is a medical device that received FDA 510(k) clearance on 2021-08-16. The listed applicant is Cpm Medical Consultants, LLC. The 510(k) number is K210695.
When did CPM Medical Consultants Tibial Revision Knee System receive FDA 510(k) clearance?
CPM Medical Consultants Tibial Revision Knee System received FDA 510(k) clearance on 2021-08-16, under 510(k) number K210695.
Who is the listed applicant for CPM Medical Consultants Tibial Revision Knee System?
The FDA 510(k) record lists Cpm Medical Consultants, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CPM Medical Consultants Tibial Revision Knee System?
The FDA product code for CPM Medical Consultants Tibial Revision Knee System is JWH.
相關臨床試驗
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相關器械(代碼:JWH)
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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