InRoad® 齿科合成骨移植
K 號：K202675 · 2022-03-04
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器材摘要
InRoad® Dental Synthetic Bone Graft is the device name listed in this FDA 510(k) record. The listed applicant is Osteogene Tech Corp. It received FDA 510(k) clearance on 2022-03-04 under 510(k) number K202675. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the InRoad® Dental Synthetic Bone Graft?
InRoad® Dental Synthetic Bone Graft is a medical device that received FDA 510(k) clearance on 2022-03-04. The listed applicant is Osteogene Tech Corp. The 510(k) number is K202675.
When did InRoad® Dental Synthetic Bone Graft receive FDA 510(k) clearance?
InRoad® Dental Synthetic Bone Graft received FDA 510(k) clearance on 2022-03-04, under 510(k) number K202675.
Who is the listed applicant for InRoad® Dental Synthetic Bone Graft?
The FDA 510(k) record lists Osteogene Tech Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InRoad® Dental Synthetic Bone Graft?
The FDA product code for InRoad® Dental Synthetic Bone Graft is LYC.
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相關器械（代碼：LYC）
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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