FDA 510(k)

自訂傳統與自訂互動式金屬牙根體

K 號：K192218 · 2020-05-08

申請人Implant Direct Sybron Manufacturing, LLC

決定日期2020-05-08

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

Custom Legacy and Custom InterActive Titanium Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Implant Direct Sybron Manufacturing, LLC. It received FDA 510(k) clearance on 2020-05-08 under 510(k) number K192218. 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 Custom Legacy and Custom InterActive Titanium Abutments?

Custom Legacy and Custom InterActive Titanium Abutments is a medical device that received FDA 510(k) clearance on 2020-05-08. The listed applicant is Implant Direct Sybron Manufacturing, LLC. The 510(k) number is K192218.

When did Custom Legacy and Custom InterActive Titanium Abutments receive FDA 510(k) clearance?

Custom Legacy and Custom InterActive Titanium Abutments received FDA 510(k) clearance on 2020-05-08, under 510(k) number K192218.

Who is the listed applicant for Custom Legacy and Custom InterActive Titanium Abutments?

The FDA 510(k) record lists Implant Direct Sybron Manufacturing, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Custom Legacy and Custom InterActive Titanium Abutments?

The FDA product code for Custom Legacy and Custom InterActive Titanium Abutments is NHA.

其他以 Implant Direct Sybron Manufacturing, LLC 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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