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# Panel to Review Sequent Aneurysm Embolization Device
- URL: https://www.fdaweb.com/panel-to-review-sequent-aneurysm-embolization-device/
- Published: 2018-08-20T12:00:00.000Z
- Updated: 2026-09-15T00:26:49.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5142151

*Federal Register* notice: FDA has announced a 9/27 Neurological Devices Panel meeting to review a Sequent Medical PMA for the Woven Endobridge (WEB) Aneurysm Embolization System, which is intended to treat wide-neck intracranial aneurysms arising or located at a vessel bifurcation. The WEB device is being evaluated in the WEB Intrasaccular Therapy Study — a multicenter, prospective, non- randomized investigation. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2018-08-20/pdf/2018-17867.pdf?ref=fdaweb.com).