FDA 510(k)

NanoBone SBX PUTTY, NanoBone QD

K 號：K190110 · 2019-04-23

決定日期2019-04-23

產品代碼MQV

諮詢委員會或

決定相當於

器材摘要

NanoBone SBX PUTTY, NanoBone QD is the device name listed in this FDA 510(k) record. The listed applicant is Artoss GmbH. It received FDA 510(k) clearance on 2019-04-23 under 510(k) number K190110. 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 NanoBone SBX PUTTY, NanoBone QD?

NanoBone SBX PUTTY, NanoBone QD is a medical device that received FDA 510(k) clearance on 2019-04-23. The listed applicant is Artoss GmbH. The 510(k) number is K190110.

When did NanoBone SBX PUTTY, NanoBone QD receive FDA 510(k) clearance?

NanoBone SBX PUTTY, NanoBone QD received FDA 510(k) clearance on 2019-04-23, under 510(k) number K190110.

Who is the listed applicant for NanoBone SBX PUTTY, NanoBone QD?

The FDA 510(k) record lists Artoss GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NanoBone SBX PUTTY, NanoBone QD?

The FDA product code for NanoBone SBX PUTTY, NanoBone QD is MQV.

其他以 Artoss GmbH 為申請人之記錄

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。

K161351NanoBone SBX 黏土

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 AG K252797JAZBI™ 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 Spine K253524Adaptos®Fuse Bone GraftBiomendex OY K253147FIBERGRAFT™ 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。