Graftys 快速設置
K 號：K231714 · 2023-07-12
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器材摘要
Graftys Quickset is the device name listed in this FDA 510(k) record. The listed applicant is Graftys. It received FDA 510(k) clearance on 2023-07-12 under 510(k) number K231714. 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 Graftys Quickset?
Graftys Quickset is a medical device that received FDA 510(k) clearance on 2023-07-12. The listed applicant is Graftys. The 510(k) number is K231714.
When did Graftys Quickset receive FDA 510(k) clearance?
Graftys Quickset received FDA 510(k) clearance on 2023-07-12, under 510(k) number K231714.
Who is the listed applicant for Graftys Quickset?
The FDA 510(k) record lists Graftys as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Graftys Quickset?
The FDA product code for Graftys Quickset is MQV.
相關臨床試驗
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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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