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FDA 510(k)

neon3™ 通用OCT脊椎穩定器

K 號：K161032 · 2016-12-22

申請人Ulrich GmbH & Co. KG
決定日期2016-12-22
產品代碼NKG
諮詢委員會或
決定相當於

器材摘要

neon3™ universal OCT spinal stabilization is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2016-12-22 under 510(k) number K161032. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the neon3™ universal OCT spinal stabilization?

neon3™ universal OCT spinal stabilization is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K161032.

When did neon3™ universal OCT spinal stabilization receive FDA 510(k) clearance?

neon3™ universal OCT spinal stabilization received FDA 510(k) clearance on 2016-12-22, under 510(k) number K161032.

Who is the listed applicant for neon3™ universal OCT spinal stabilization?

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

What is the FDA product code for neon3™ universal OCT spinal stabilization?

The FDA product code for neon3™ universal OCT spinal stabilization is NKG.

相關臨床試驗

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其他以 Ulrich GmbH & Co. KG 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。

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相關器械（代碼：NKG）

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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