FDA 510(k)

頭蓋骨钻頭及配件

K 號：K170442 · 2017-09-07

申請人Ad-Tech Medical Instrument Corporation

決定日期2017-09-07

產品代碼HBE

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Cranial Drill Bits and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Ad-Tech Medical Instrument Corporation. It received FDA 510(k) clearance on 2017-09-07 under 510(k) number K170442. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cranial Drill Bits and Accessories?

Cranial Drill Bits and Accessories is a medical device that received FDA 510(k) clearance on 2017-09-07. The listed applicant is Ad-Tech Medical Instrument Corporation. The 510(k) number is K170442.

When did Cranial Drill Bits and Accessories receive FDA 510(k) clearance?

Cranial Drill Bits and Accessories received FDA 510(k) clearance on 2017-09-07, under 510(k) number K170442.

Who is the listed applicant for Cranial Drill Bits and Accessories?

The FDA 510(k) record lists Ad-Tech Medical Instrument Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cranial Drill Bits and Accessories?

The FDA product code for Cranial Drill Bits and Accessories is HBE.

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相關器械（代碼：HBE）

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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