Artus™ cervical plate system
K 號：K202227 · 2020-09-14
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器材摘要
Artus™ cervical plate system is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2020-09-14 under 510(k) number K202227. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Artus™ cervical plate system?
Artus™ cervical plate system is a medical device that received FDA 510(k) clearance on 2020-09-14. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K202227.
When did Artus™ cervical plate system receive FDA 510(k) clearance?
Artus™ cervical plate system received FDA 510(k) clearance on 2020-09-14, under 510(k) number K202227.
Who is the listed applicant for Artus™ cervical plate system?
The FDA 510(k) record lists Ulrich GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Artus™ cervical plate system?
The FDA product code for Artus™ cervical plate system is KWQ.
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其他以 Ulrich GmbH & Co. KG 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。
K252281ulricheasyINJECT Max 2M (XD 10140)；ulricheasyINJECT Max 3 (XD 10150)；ulricheasyINJECT Max 3 (XD 10180)K251295烏爾里希注射CT動態 (XD 8000)K241850ulricheasyINJECT Max 2M (XD 10140)；ulricheasyINJECT Max 3 (XD 10150)；ulricheasyINJECT Max 3 (XD 10180)K233737ulricheasyINJECT Max 2M (XD 10140)；ulricheasyINJECT Max 3 (XD 10150)；ulricheasyINJECT Max 3 (XD 10180)K210541烏爾里希注射CT移動K192872烏爾里希注射CT動態
相關器械（代碼：KWQ）
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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