FDA 510(k)

InCore TMT 系統

K 號：K192578 · 2019-12-31

決定日期2019-12-31

產品代碼HWC

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決定相當於

器材摘要

InCore TMT System is the device name listed in this FDA 510(k) record. The listed applicant is Nextremity Solutions, Inc.. It received FDA 510(k) clearance on 2019-12-31 under 510(k) number K192578. 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 InCore TMT System?

InCore TMT System is a medical device that received FDA 510(k) clearance on 2019-12-31. The listed applicant is Nextremity Solutions, Inc.. The 510(k) number is K192578.

When did InCore TMT System receive FDA 510(k) clearance?

InCore TMT System received FDA 510(k) clearance on 2019-12-31, under 510(k) number K192578.

Who is the listed applicant for InCore TMT System?

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

What is the FDA product code for InCore TMT System?

The FDA product code for InCore TMT System is HWC. This falls under the Cardiovascular category.

其他以 Nextremity Solutions, 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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