Coils
VortX - 18
by Boston Scientific Corporation
A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
VortX - 18 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 |
|---|---|---|---|
| M0013812040 | — | MR Conditional | Available |
Procedures that use coils
Frequently asked questions
What is VortX - 18 used for?
A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; 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 VortX - 18?
VortX - 18 is made by Boston Scientific Corporation. It is listed under embolization coils in our device library.
What sizes does VortX - 18 come in?
The FDA device database does not list sizes for VortX - 18. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is VortX - 18 MRI safe?
The FDA device database lists VortX - 18 as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is VortX - 18 FDA cleared?
VortX - 18 is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Boston Scientific Corporation sales representative?
Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation 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.