免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA PMA

組織移植片,直徑6mm以上

PMA 核准號:P020049 · 2018-09-28

決定日期2018-09-28
PMA 編號P020049
產品代碼LXA
器械分類3 類
醫療專科U
諮詢委員會履歷

器材摘要

Tissue graft of 6mm and greater is the device name listed in this FDA 510(k) record. The listed applicant is LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2018-09-28. The device is classified under product code LXA. It was reviewed by the CV advisory panel.

常見問題

What is the Tissue graft of 6mm and greater?

Tissue graft of 6mm and greater is a medical device that received FDA 510(k) clearance on 2018-09-28. The listed applicant is LeMaitre Vascular, Inc..

When did Tissue graft of 6mm and greater receive FDA 510(k) clearance?

The clearance date for Tissue graft of 6mm and greater can be found in the official FDA records.

誰是6mm以上組織移植的登記申請人?

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

FDA產品代碼為6mm以上組織移植物是什麼?

FDA產品代碼,6mm以上組織移植為LXA。

相關臨床試驗

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。

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。

↑