FDA 510(k)

Medline UNITE®數位融合螺釘系統

K 號：K211944 · 2021-07-22

決定日期2021-07-22

產品代碼HWC

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器材摘要

Medline UNITE® Digital Fusion Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2021-07-22 under 510(k) number K211944. 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 Medline UNITE® Digital Fusion Screw System?

Medline UNITE® Digital Fusion Screw System is a medical device that received FDA 510(k) clearance on 2021-07-22. The listed applicant is Medline Industries, Inc.. The 510(k) number is K211944.

When did Medline UNITE® Digital Fusion Screw System receive FDA 510(k) clearance?

Medline UNITE® Digital Fusion Screw System received FDA 510(k) clearance on 2021-07-22, under 510(k) number K211944.

Who is the listed applicant for Medline UNITE® Digital Fusion Screw System?

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

What is the FDA product code for Medline UNITE® Digital Fusion Screw System?

The FDA product code for Medline UNITE® Digital Fusion Screw System is HWC. This falls under the Cardiovascular category.

其他以 Medline Industries, 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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