FDA 510(k)

魔法 UCLA 牙槽系統

K 號：K202418 · 2020-12-03

決定日期2020-12-03

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

Magic UCLA Abutment System is the device name listed in this FDA 510(k) record. The listed applicant is Innobiosurg Co., Ltd.. It received FDA 510(k) clearance on 2020-12-03 under 510(k) number K202418. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Magic UCLA Abutment System?

Magic UCLA Abutment System is a medical device that received FDA 510(k) clearance on 2020-12-03. The listed applicant is Innobiosurg Co., Ltd.. The 510(k) number is K202418.

When did Magic UCLA Abutment System receive FDA 510(k) clearance?

Magic UCLA Abutment System received FDA 510(k) clearance on 2020-12-03, under 510(k) number K202418.

Who is the listed applicant for Magic UCLA Abutment System?

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

What is the FDA product code for Magic UCLA Abutment System?

The FDA product code for Magic UCLA Abutment System is NHA.

其他以 Innobiosurg Co., Ltd. 為申請人之記錄

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相關器械（代碼：NHA）

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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