DePuy Synthes 矢狹板固定系統
K 號：K233967 · 2024-05-09
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器材摘要
DePuy Synthes MatrixSTERNUM Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Synthes GmbH. It received FDA 510(k) clearance on 2024-05-09 under 510(k) number K233967. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DePuy Synthes MatrixSTERNUM Fixation System?
DePuy Synthes MatrixSTERNUM Fixation System is a medical device that received FDA 510(k) clearance on 2024-05-09. The listed applicant is Synthes GmbH. The 510(k) number is K233967.
When did DePuy Synthes MatrixSTERNUM Fixation System receive FDA 510(k) clearance?
DePuy Synthes MatrixSTERNUM Fixation System received FDA 510(k) clearance on 2024-05-09, under 510(k) number K233967.
Who is the listed applicant for DePuy Synthes MatrixSTERNUM Fixation System?
The FDA 510(k) record lists Synthes GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DePuy Synthes MatrixSTERNUM Fixation System?
The FDA product code for DePuy Synthes MatrixSTERNUM Fixation System is HRS.
相關臨床試驗
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其他以 Synthes 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：HRS）
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。
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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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