骨質3 ZP 黏土
K 號：K193075 · 2020-06-09
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器材摘要
Osteo3 ZP Putty is the device name listed in this FDA 510(k) record. The listed applicant is Sirakoss , Ltd.. It received FDA 510(k) clearance on 2020-06-09 under 510(k) number K193075. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Osteo3 ZP Putty?
Osteo3 ZP Putty is a medical device that received FDA 510(k) clearance on 2020-06-09. The listed applicant is Sirakoss , Ltd.. The 510(k) number is K193075.
When did Osteo3 ZP Putty receive FDA 510(k) clearance?
Osteo3 ZP Putty received FDA 510(k) clearance on 2020-06-09, under 510(k) number K193075.
Who is the listed applicant for Osteo3 ZP Putty?
The FDA 510(k) record lists Sirakoss , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Osteo3 ZP Putty?
The FDA product code for Osteo3 ZP Putty is MQV.
相關臨床試驗
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：MQV）
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
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