FDA PMA

STENT, ILIAC

PMA Number: P110011 · 2017-02-01

ApplicantMedtronic, Ireland

Decision Date2017-02-01

PMA NumberP110011

Product CodeNIO

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeCV

Device Summary

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.

Frequently Asked Questions

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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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.