K3
K 號：K183347 · 2019-09-04
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器材摘要
K3 is the device name listed in this FDA 510(k) record. The listed applicant is Osstem Implant Co., Ltd.. It received FDA 510(k) clearance on 2019-09-04 under 510(k) number K183347. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the K3?
K3 is a medical device that received FDA 510(k) clearance on 2019-09-04. The listed applicant is Osstem Implant Co., Ltd.. The 510(k) number is K183347.
When did K3 receive FDA 510(k) clearance?
K3 received FDA 510(k) clearance on 2019-09-04, under 510(k) number K183347.
Who is the listed applicant for K3?
The FDA 510(k) record lists Osstem Implant Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for K3?
The FDA product code for K3 is EIA.
其他以 Osstem Implant Co., Ltd. 為申請人之記錄
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相關器械（代碼：EIA）
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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