FDA 510(k)

Arco®-SA 腰椎籠架系統

K 號：K182195 · 2018-11-09

決定日期2018-11-09

產品代碼OVD

諮詢委員會或

決定相當於

器材摘要

Arco™-SA Lumbar Cage System is the device name listed in this FDA 510(k) record. The listed applicant is Neurostructures, Inc.. It received FDA 510(k) clearance on 2018-11-09 under 510(k) number K182195. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Arco™-SA Lumbar Cage System?

Arco™-SA Lumbar Cage System is a medical device that received FDA 510(k) clearance on 2018-11-09. The listed applicant is Neurostructures, Inc.. The 510(k) number is K182195.

When did Arco™-SA Lumbar Cage System receive FDA 510(k) clearance?

Arco™-SA Lumbar Cage System received FDA 510(k) clearance on 2018-11-09, under 510(k) number K182195.

Who is the listed applicant for Arco™-SA Lumbar Cage System?

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

What is the FDA product code for Arco™-SA Lumbar Cage System?

The FDA product code for Arco™-SA Lumbar Cage System is OVD.

其他以 Neurostructures, Inc. 為申請人之記錄

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相關器械（代碼：OVD）

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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