骨關節連接器
K 號：K223563 · 2023-01-25
廣告
器材摘要
OsteoCNX is the device name listed in this FDA 510(k) record. The listed applicant is Converg Engineering. It received FDA 510(k) clearance on 2023-01-25 under 510(k) number K223563. 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 OsteoCNX?
OsteoCNX is a medical device that received FDA 510(k) clearance on 2023-01-25. The listed applicant is Converg Engineering. The 510(k) number is K223563.
When did OsteoCNX receive FDA 510(k) clearance?
OsteoCNX received FDA 510(k) clearance on 2023-01-25, under 510(k) number K223563.
Who is the listed applicant for OsteoCNX?
The FDA 510(k) record lists Converg Engineering as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OsteoCNX?
The FDA product code for OsteoCNX 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。
K262230Mg 骨回復™；Mg 骨凝合™Bone Solutions, Inc.K260364設備 300419 識別條Geistlich Pharma AGK252797JAZBI™ 可吸收骨空洞填充物Sdip Innovations Pty, Ltd.K261008Vitoss® BiModal 生物活性骨移植代用品泡沫條；Vitoss® BiModal 生物活性骨移植代用品；Vitoss BBTrauma® 生物活性骨移植代用品；Vitoss® BA2X 生物活性骨移植代用品；Vitoss® 生物活性泡沫骨移植代用品包；Vitoss® 生物活性泡沫骨移植代用品；Vitoss® 泡沫骨移植代用品；Vitoss® 骨移植代用品填充罐；Vitoss® 骨移植代用品Stryker SpineK253524Adaptos®Fuse Bone GraftBiomendex OYK253147FIBERGRAFT™ BG 黏土 GPS 骨移植代用品 FIBERGRAFT™ BG 黏土 骨移植代用品 FIBERGRAFT™ AERIDYAN™ 維網骨移植代用品 FIBERGRAFT™ BG 維網骨移植代用品Prosidyan, Inc.
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。
廣告