FDA PMA

STENT, ILIAC

Número do PMA: P110011 · 2017-02-01

RequerenteMedtronic, Ireland

Data da decisão2017-02-01

Número PMAP110011

Código do produtoNIO

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoCV

Resumo do dispositivo

STENT, ILIAC is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Ireland. It received FDA 510(k) clearance on 2017-02-01. The device is classified under product code NIO. It was reviewed by the CV advisory panel.

Perguntas frequentes

What is the STENT, ILIAC?

STENT, ILIAC is a medical device that received FDA 510(k) clearance on 2017-02-01. The listed applicant is Medtronic, Ireland.

When did STENT, ILIAC receive FDA 510(k) clearance?

The clearance date for STENT, ILIAC can be found in the official FDA records.

Who is the listed applicant for STENT, ILIAC?

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

What is the FDA product code for STENT, ILIAC?

The FDA product code for STENT, ILIAC is NIO.

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