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November 16, 2021; 97 (20 Supplement 2) Future Directions

Food and Drug Association Approval Process for Devices Used in Endovascular Treatment of Stroke

Shreyas Gangadhara, Adnan Siddiqui, Maxim Mokin
First published November 16, 2021, DOI: https://doi.org/10.1212/WNL.0000000000012804
Shreyas Gangadhara
From the Department of Neurology (S.G.), University of Mississippi Medical Center, Jackson; Department of Neurosurgery (A.S.), University at Buffalo, NY; and Department of Neurosurgery and Brain Repair (M.M.), University of South Florida, Tampa.
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Adnan Siddiqui
From the Department of Neurology (S.G.), University of Mississippi Medical Center, Jackson; Department of Neurosurgery (A.S.), University at Buffalo, NY; and Department of Neurosurgery and Brain Repair (M.M.), University of South Florida, Tampa.
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Maxim Mokin
From the Department of Neurology (S.G.), University of Mississippi Medical Center, Jackson; Department of Neurosurgery (A.S.), University at Buffalo, NY; and Department of Neurosurgery and Brain Repair (M.M.), University of South Florida, Tampa.
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Citation
Food and Drug Association Approval Process for Devices Used in Endovascular Treatment of Stroke
Shreyas Gangadhara, Adnan Siddiqui, Maxim Mokin
Neurology Nov 2021, 97 (20 Supplement 2) S194-S200; DOI: 10.1212/WNL.0000000000012804

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Abstract

Purpose of the Review This article reviews the Food and Drug Administration's (FDA’s) process for approval of new medical devices and describes the evolution of endovascular devices used for the treatment of acute ischemic stroke.

Recent Findings Several recent studies have established the benefit of endovascular treatment of acute ischemic stroke from emergent large vessel occlusion. This has led to endovascular treatment becoming the usual care in acute stroke management and has generated greater-than-ever interest in the development of newer and more effective devices.

Summary In the United States, the FDA is the regulatory authority that is empowered with the approval and monitoring of new medical devices for widespread use in the population. The FDA categorizes medical devices into 3 classes based mainly on their potential risks to patients and/or users; class I devices pose the least risk and have the least stringent approval process, while class III devices pose the highest risk and undergo the most stringent and time-consuming approval process. There are 4 main pathways to approval: premarket notification, also known as the 510(k) pathway; premarket approval (PMA), de novo, and Humanitarian Device Exemption pathway. These pathways are described in detail in the article. The FDA also mandates postmarketing surveillance to identify any untoward and unexpected long-term complications.

Glossary

FDA=
Food and Drug Administration;
HDE=
Humanitarian Device Exemption;
HUD=
Humanitarian Use Device;
PMA=
premarket approval;
PMN=
premarket notification;
SAMMPRIS=
Stenting and Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis;
WASID=
Warfarin-Aspirin Symptomatic Intracranial Disease

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received June 28, 2020.
  • Accepted in final form February 24, 2021.
  • © 2021 American Academy of Neurology
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