SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
PMA番号：P070007 · 2016-04-05
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医療機器の概要
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2016-04-05. The device is classified under product code MIH. It was reviewed by the CV advisory panel.
よくある質問
What is the SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT?
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT is a medical device that received FDA 510(k) clearance on 2016-04-05. The listed applicant is Medtronic Vascular.
When did SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT receive FDA 510(k) clearance?
The clearance date for SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT can be found in the official FDA records.
Who is the listed applicant for SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT?
The FDA product code for SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT is MIH.
関連する臨床試験
関連レコードは、名称、製品コード、その他のメタデータを使用して自動的にマッチングされます。マッチは検証された臨床的、科学的、企業的、または規制上の関係を確立するものではありません。リンクされた公式情報源をご確認ください。
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公式ソース
FDAデータベースで見る →データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。
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