FDA 510(k)

增強外科機器人系統

K 號：K171120 · 2017-10-13

決定日期2017-10-13

產品代碼NAY

諮詢委員會GU

決定相當於

器材摘要

Senhance Surgical Robotic System is the device name listed in this FDA 510(k) record. The listed applicant is Transenterix, Inc.. It received FDA 510(k) clearance on 2017-10-13 under 510(k) number K171120. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Senhance Surgical Robotic System?

Senhance Surgical Robotic System is a medical device that received FDA 510(k) clearance on 2017-10-13. The listed applicant is Transenterix, Inc.. The 510(k) number is K171120.

When did Senhance Surgical Robotic System receive FDA 510(k) clearance?

Senhance Surgical Robotic System received FDA 510(k) clearance on 2017-10-13, under 510(k) number K171120.

Who is the listed applicant for Senhance Surgical Robotic System?

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

What is the FDA product code for Senhance Surgical Robotic System?

The FDA product code for Senhance Surgical Robotic System is NAY.

其他以 Transenterix, Inc. 為申請人之記錄

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相關器械（代碼：NAY）

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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官方來源

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