FDA 510(k)

卡西洛夫脊椎板系統

K 號：K203154 · 2020-11-05

決定日期2020-11-05

產品代碼KWQ

諮詢委員會或

決定相當於

器材摘要

KASILOF Cervical Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Kahtnu Surgical, Inc.. It received FDA 510(k) clearance on 2020-11-05 under 510(k) number K203154. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the KASILOF Cervical Plate System?

KASILOF Cervical Plate System is a medical device that received FDA 510(k) clearance on 2020-11-05. The listed applicant is Kahtnu Surgical, Inc.. The 510(k) number is K203154.

When did KASILOF Cervical Plate System receive FDA 510(k) clearance?

KASILOF Cervical Plate System received FDA 510(k) clearance on 2020-11-05, under 510(k) number K203154.

Who is the listed applicant for KASILOF Cervical Plate System?

The FDA 510(k) record lists Kahtnu Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KASILOF Cervical Plate System?

The FDA product code for KASILOF Cervical Plate System is KWQ.

其他以 Kahtnu Surgical, Inc. 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。

K213115CHENA-C 间隔系統

相關器械（代碼：KWQ）

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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