植床地
K 號：K173110 · 2018-05-18
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器材摘要
GRAFTSITE is the device name listed in this FDA 510(k) record. The listed applicant is Summit Medical , Ltd.. It received FDA 510(k) clearance on 2018-05-18 under 510(k) number K173110. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the GRAFTSITE?
GRAFTSITE is a medical device that received FDA 510(k) clearance on 2018-05-18. The listed applicant is Summit Medical , Ltd.. The 510(k) number is K173110.
When did GRAFTSITE receive FDA 510(k) clearance?
GRAFTSITE received FDA 510(k) clearance on 2018-05-18, under 510(k) number K173110.
Who is the listed applicant for GRAFTSITE?
The FDA 510(k) record lists Summit Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRAFTSITE?
The FDA product code for GRAFTSITE is BSP.
相關臨床試驗
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其他以 Summit Medical , Ltd. 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。
相關器械（代碼：BSP）
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。
K243690SonoMSKPAJUNK GmbH MedizintechnologieK243682SonoPlex STIM；SonoPlex IIPAJUNK GmbH MedizintechnologieK250774SPROTTE® 标準 (LUER/NRFit®) 腰椎穿刺PAJUNK GmbH MedizintechnologieK243525SonoTAP 及 SonoTAP IIPAJUNK GmbH MedizintechnologieK241953SPROTTE®標準（LUER/NRFit®）麻醉學PAJUNK GmbH MedizintechnologieK241954SonoBlock；SonoBlock IIPAJUNK GmbH Medizintechnologie
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。
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