FDA 510(k)

CREED™ 穿刺螺釘

K 號：K223847 · 2023-01-25

決定日期2023-01-25

產品代碼HWC

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決定相當於

器材摘要

CREED™ Cannulated Screws is the device name listed in this FDA 510(k) record. The listed applicant is Glw, Inc.. It received FDA 510(k) clearance on 2023-01-25 under 510(k) number K223847. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the CREED™ Cannulated Screws?

CREED™ Cannulated Screws is a medical device that received FDA 510(k) clearance on 2023-01-25. The listed applicant is Glw, Inc.. The 510(k) number is K223847.

When did CREED™ Cannulated Screws receive FDA 510(k) clearance?

CREED™ Cannulated Screws received FDA 510(k) clearance on 2023-01-25, under 510(k) number K223847.

Who is the listed applicant for CREED™ Cannulated Screws?

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

What is the FDA product code for CREED™ Cannulated Screws?

The FDA product code for CREED™ Cannulated Screws is HWC. This falls under the Cardiovascular category.

其他以 Glw, Inc. 為申請人之記錄

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相關器械（代碼：HWC）

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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