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FDA 510(k)

TECHFIT DISRP® 系統

K 號：K230276 · 2023-06-23

申請人Techfit Digital Surgery
決定日期2023-06-23
產品代碼DZJ
諮詢委員會DE
決定相當於

器材摘要

TECHFIT DISRP® System is the device name listed in this FDA 510(k) record. The listed applicant is Techfit Digital Surgery. It received FDA 510(k) clearance on 2023-06-23 under 510(k) number K230276. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the TECHFIT DISRP® System?

TECHFIT DISRP® System is a medical device that received FDA 510(k) clearance on 2023-06-23. The listed applicant is Techfit Digital Surgery. The 510(k) number is K230276.

When did TECHFIT DISRP® System receive FDA 510(k) clearance?

TECHFIT DISRP® System received FDA 510(k) clearance on 2023-06-23, under 510(k) number K230276.

Who is the listed applicant for TECHFIT DISRP® System?

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

What is the FDA product code for TECHFIT DISRP® System?

The FDA product code for TECHFIT DISRP® System is DZJ.

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

相關器械（代碼：DZJ）

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。

K261826VSP系統（鈦金顎板牙橋）3D Systems, Inc.K243637Materialise個人化頭顱顏面手術導引和模型Materialise NVK242263TECHFIT DISRP® 系統Techfit Digital Surgery, Inc.K231520tmCMF解決方案Techmah CmfK223024MedCAD精準計劃系統MedcadK220366嵌入式醫療設備3D Lifeprints UK , Ltd.

官方來源

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