FDA 510(k)

Nano FortiFix® 系統

K 號：K193211 · 2020-03-20

決定日期2020-03-20

產品代碼NKB

諮詢委員會或

決定相當於

器材摘要

Nano FortiFix® System is the device name listed in this FDA 510(k) record. The listed applicant is Nanovis Spine, LLC. It received FDA 510(k) clearance on 2020-03-20 under 510(k) number K193211. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Nano FortiFix® System?

Nano FortiFix® System is a medical device that received FDA 510(k) clearance on 2020-03-20. The listed applicant is Nanovis Spine, LLC. The 510(k) number is K193211.

When did Nano FortiFix® System receive FDA 510(k) clearance?

Nano FortiFix® System received FDA 510(k) clearance on 2020-03-20, under 510(k) number K193211.

Who is the listed applicant for Nano FortiFix® System?

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

What is the FDA product code for Nano FortiFix® System?

The FDA product code for Nano FortiFix® System is NKB.

其他以 Nanovis Spine, LLC 為申請人之記錄

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相關器械（代碼：NKB）

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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