馬格尼斯-C 頸椎前方板系統
K 號：K221053 · 2023-03-01
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器材摘要
Magnes-C Anterior Cervical Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Fellowship of Orthopaedic Researchers, Inc.. It received FDA 510(k) clearance on 2023-03-01 under 510(k) number K221053. 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 Magnes-C Anterior Cervical Plate System?
Magnes-C Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2023-03-01. The listed applicant is Fellowship of Orthopaedic Researchers, Inc.. The 510(k) number is K221053.
When did Magnes-C Anterior Cervical Plate System receive FDA 510(k) clearance?
Magnes-C Anterior Cervical Plate System received FDA 510(k) clearance on 2023-03-01, under 510(k) number K221053.
Who is the listed applicant for Magnes-C Anterior Cervical Plate System?
The FDA 510(k) record lists Fellowship of Orthopaedic Researchers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Magnes-C Anterior Cervical Plate System?
The FDA product code for Magnes-C Anterior Cervical Plate System is KWQ.
相關臨床試驗
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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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