高貴植入系統
K 號：K240383 · 2024-10-31
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器材摘要
Highness Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Highness Co., Ltd.. It received FDA 510(k) clearance on 2024-10-31 under 510(k) number K240383. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Highness Implant System?
Highness Implant System is a medical device that received FDA 510(k) clearance on 2024-10-31. The listed applicant is Highness Co., Ltd.. The 510(k) number is K240383.
When did Highness Implant System receive FDA 510(k) clearance?
Highness Implant System received FDA 510(k) clearance on 2024-10-31, under 510(k) number K240383.
Who is the listed applicant for Highness Implant System?
The FDA 510(k) record lists Highness Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Highness Implant System?
The FDA product code for Highness Implant System is DZE.
相關臨床試驗
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相關器械（代碼：DZE）
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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