WEB devices
WEB Aneurysm Embolization System
A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Where to buy WEB Aneurysm Embolization System
We do not have contact details for Sequent Medical, Inc. yet. Send a request and we will route it to the right person for your country.
WEB Aneurysm Embolization System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| W2-8-3 | — | MR Conditional | Available |
| W2-8-4 | — | MR Conditional | Available |
| W2-8-5 | — | MR Conditional | Available |
| W2-8-6 | — | MR Conditional | Available |
| W2-8-7 | — | MR Conditional | Available |
| W2-8-S | — | MR Conditional | Available |
| W2-9-4 | — | MR Conditional | Available |
| W2-9-5 | — | MR Conditional | Available |
| W2-9-6 | — | MR Conditional | Available |
| W2-9-7 | — | MR Conditional | Available |
| W2-9-8 | — | MR Conditional | Available |
| W2-9-S | — | MR Conditional | Available |
| W2-10-5 | — | MR Conditional | Available |
| W2-10-6 | — | MR Conditional | Available |
| W2-10-7 | — | MR Conditional | Available |
| W2-10-8 | — | MR Conditional | Available |
| W2-10-S | — | MR Conditional | Available |
| W2-11-6 | — | MR Conditional | Available |
| W2-11-7 | — | MR Conditional | Available |
| W2-11-8 | — | MR Conditional | Available |
| W2-11-9 | — | MR Conditional | Available |
| W2-11-S | — | MR Conditional | Available |
| W4-4-3 | — | MR Conditional | Available |
| W4-4-4 | — | MR Conditional | Available |
| W4-4-S | — | MR Conditional | Available |
| W4-5-3 | — | MR Conditional | Available |
| W4-5-4 | — | MR Conditional | Available |
| W4-5-5 | — | MR Conditional | Available |
| W4-5-S | — | MR Conditional | Available |
| W4-6-3 | — | MR Conditional | Available |
| W4-6-4 | — | MR Conditional | Available |
| W4-6-5 | — | MR Conditional | Available |
| W4-6-6 | — | MR Conditional | Available |
| W4-6-S | — | MR Conditional | Available |
| W4-7-3 | — | MR Conditional | Available |
| W4-7-4 | — | MR Conditional | Available |
| W4-7-5 | — | MR Conditional | Available |
| W4-7-6 | — | MR Conditional | Available |
| W4-7-S | — | MR Conditional | Available |
FDA clearances
- PMA P170032 January 2021
Procedures that use web devices
Frequently asked questions
What is WEB Aneurysm Embolization System used for?
A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Who makes WEB Aneurysm Embolization System?
WEB Aneurysm Embolization System is made by Sequent Medical, Inc.. It is listed under intrasaccular flow disruption devices (web) in our device library.
What sizes does WEB Aneurysm Embolization System come in?
The FDA device database does not list sizes for WEB Aneurysm Embolization System. Check the instructions for use or ask a Sequent Medical, Inc. representative.
Is WEB Aneurysm Embolization System MRI safe?
The FDA device database lists WEB Aneurysm Embolization System as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is WEB Aneurysm Embolization System FDA cleared?
WEB Aneurysm Embolization System is covered by FDA submission P170032.
How do I contact a Sequent Medical, Inc. sales representative?
Sequent Medical, Inc. has not listed representatives on LA Vascular yet. Visit the Sequent Medical, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.