Versius Surgical System (Versius Plus)
K 號：K252111 · 2025-12-16
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器材摘要
Versius Surgical System (Versius Plus) is the device name listed in this FDA 510(k) record. The listed applicant is Cmr Surgical Limited. It received FDA 510(k) clearance on 2025-12-16 under 510(k) number K252111. The device is classified under product code SCV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Versius Surgical System (Versius Plus)?
Versius Surgical System (Versius Plus) is a medical device that received FDA 510(k) clearance on 2025-12-16. The listed applicant is Cmr Surgical Limited. The 510(k) number is K252111.
When did Versius Surgical System (Versius Plus) receive FDA 510(k) clearance?
Versius Surgical System (Versius Plus) received FDA 510(k) clearance on 2025-12-16, under 510(k) number K252111.
Who is the listed applicant for Versius Surgical System (Versius Plus)?
The FDA 510(k) record lists Cmr Surgical Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Versius Surgical System (Versius Plus)?
The FDA product code for Versius Surgical System (Versius Plus) is SCV.
相關臨床試驗
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相關器械（代碼：SCV）
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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