FDA PMA

STENT, ILIAC

PMA Number: P030045 · 2024-07-26

ApplicantMedtronic Vascular, Inc.

Decision Date2024-07-26

PMA NumberP030045

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 Vascular, Inc.. It received FDA 510(k) clearance on 2024-07-26. 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 2024-07-26. The listed applicant is Medtronic Vascular, Inc..

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 Vascular, Inc. 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.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

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.