Medtronic Receives U.S. FDA Approval for Pipeline™ Flex Embolization Device with Shield Technology™

Rhea-AI Summary

Medtronic has received FDA approval for its Pipeline™ Flex Embolization Device with Shield Technology, designed to enhance flow diversion therapy for brain aneurysms. The first patient procedure was performed at NYU Langone Health. This device, a market leader for a decade, reduces thrombogenicity, facilitating better delivery through complex vascular anatomy. Clinical results show a 77.2% complete aneurysm occlusion rate at 12 months, and improvements in safety and efficacy. The advancement marks a significant milestone in treating cerebral aneurysms, aiming to improve patient outcomes.

Positive

• FDA approval received for Pipeline Flex Embolization Device with Shield Technology.
• First patient procedure successfully conducted at NYU Langone Health.
• 77.2% complete aneurysm occlusion at 12 months, demonstrating superior efficacy.
• Reduces thrombogenicity, enhancing device performance and patient outcomes.

Negative

• None.

First Patient Receives New Shield Surface Modification, An Advance in Flow Diversion Therapy, at NYU Langone Health

DUBLIN, April 21, 2021 /PRNewswire/ -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced it has received approval from the United States Food and Drug Administration (FDA) for Pipeline™ Flex Embolization Device with Shield Technology™. Medtronic developed Shield Technology, a proprietary breakthrough in biomaterial science, to advance flow diversion therapy by introducing the first surface-modified implant device which demonstrates reduction in material thrombogenicity, a reduction in the tendency of the surface treatment material to create clots. NYU Langone Health in New York City performed the first patient procedure in the nation with the new device.

Celebrating its 10-year anniversary in the U.S. in 2021, Pipeline Flex Embolization Device diverts blood flow away from a brain aneurysm. The first commercially available flow diverter in the market, the device features a braided cylindrical mesh tube that is implanted across the base, or neck, of the aneurysm. The device interrupts blood flow into the aneurysm, reconstructing the diseased section of the parent vessel. Pre-clinical testing shows how Shield Technology improves Pipeline Flex by reducing the thrombogenicity of the device material.

"The Pipeline Flex-Shield that we used today at NYU Langone to treat a giant left internal carotid aneurysm, represents a pivotal milestone in the evolution of flow diversion therapy—establishing a new vanguard for safe and effective management of complex cerebral aneurysms," said Peter Kim Nelson, M.D., chief of Interventional Neuroradiology and professor of Radiology and Neurosurgery at NYU Langone Health. "Our team has long-anticipated the availability of this device for patients in the United States. The surface modification of the implant has demonstrated reduced material thrombogenicity,  discernably aiding delivery through tortuous vascular anatomy with improved delivery and resheathing forces compared to earlier generation flow diverters."

Published on June 1, 2020, in the Journal of NeuroInterventional Surgery (JNIS), results from the SHIELD Study (Periprocedural to 1-year safety and efficacy outcomes with the Pipeline Embolization Device with Shield technology for intracranial aneurysms: a prospective, post-market, multi-center study) demonstrate that the third-generation Pipeline Flex Embolization Device with Shield Technology continues the strong record of safety and efficacy of flow diversion therapy with the Medtronic family of products. Results show 77.2% complete aneurysm occlusion at 12 months, a 3.2% primary safety endpoint, and 93.1% complete wall apposition post-procedure.

"In addition to addressing material thrombogenicity, Shield Technology improves device performance  by reducing the force required for both delivery and resheathing of the device. We believe that Shield Technology opens up a new range of options for physicians to continue to achieve improved patient outcomes," said Dan Volz, president of the Neurovascular business, which is part of the Neuroscience Portfolio at Medtronic. "Ten years ago, Medtronic changed the treatment paradigm in brain aneurysms with the approval of Pipeline Embolization Device, and we continue to challenge ourselves to deliver solutions that improve outcomes and increase value for all healthcare stakeholders."

An estimated 500,000 people throughout the world die each year due to ruptured brain aneurysms, with half the victims younger than 50 years of age. As the most studied flow diverter worldwide, Pipeline Embolization Device has been used to treat patients in the United States since 2011 and is now available with Shield Technology.

"Brain aneurysms are much more common than most people believe and require early detection, accurate diagnosis, and prompt treatment to maximize the chances of survival," said Todd Crawford, founder, Lisa Foundation, dedicated to his wife Lisa who lost her life to complications from a brain aneurysm. "As a valued partner who shared our mission, we commend Medtronic for its continued commitment to pioneering new therapies and approaches to treating brain aneurysms that improve patient outcomes and saves lives."

Dr. Nelson reports no disclosures with Medtronic.

About Medtronic
Medtronic plc (www.medtronic.com), headquartered in Dublin, Ireland, is among the world's largest medical technology, services, and solutions companies – alleviating pain, restoring health, and extending life for millions of people around the world. Medtronic employs more than 90,000 people worldwide, serving physicians, hospitals, and patients in more than 150 countries. The company is focused on collaborating with stakeholders around the world to take healthcare Further, Together.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

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SOURCE Medtronic plc

FAQ

What is the significance of the FDA approval for MDT on April 21, 2021?

The FDA approval for Medtronic's Pipeline Flex Embolization Device with Shield Technology highlights its advancement in treating brain aneurysms and aims to improve patient outcomes.

What are the benefits of the Pipeline Flex Embolization Device with Shield Technology?

The device reduces thrombogenicity, enhances delivery through complex vascular anatomy, and has shown a 77.2% complete aneurysm occlusion rate at 12 months.

When was the first patient treated with the new Pipeline Flex device?

The first patient procedure using the Pipeline Flex Embolization Device with Shield Technology was performed at NYU Langone Health on April 21, 2021.

What clinical results support the effectiveness of MDT's new device?

Clinical results show a 77.2% complete aneurysm occlusion rate at 12 months and a 3.2% primary safety endpoint.

How does Shield Technology improve the Pipeline Flex device?

Shield Technology reduces the force required for delivery and resheathing while decreasing material thrombogenicity, resulting in enhanced performance.