c1Trac
K 號：K222912 · 2023-05-16
廣告
器材摘要
c1Trac is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2023-05-16 under 510(k) number K222912. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the c1Trac?
c1Trac is a medical device that received FDA 510(k) clearance on 2023-05-16. The listed applicant is Zimmer Medizinsysteme GmbH. The 510(k) number is K222912.
When did c1Trac receive FDA 510(k) clearance?
c1Trac received FDA 510(k) clearance on 2023-05-16, under 510(k) number K222912.
Who is the listed applicant for c1Trac?
The FDA 510(k) record lists Zimmer Medizinsysteme GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for c1Trac?
The FDA product code for c1Trac is ITH.
其他以 Zimmer Medizinsysteme GmbH 為申請人之記錄
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。
相關器械（代碼：ITH）
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。
廣告