Coils
swiftMATCH Coil, Soft
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.
swiftMATCH Coil, Soft 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 |
|---|---|---|---|
| 400SWSFT306-A | Length 6 cm | MR Conditional | Available |
| 400SWSFT406-A | Length 6 cm | MR Conditional | Available |
| 400SWSFT410-A | Length 10 cm | MR Conditional | Available |
| 400SWSFT510-A | Length 10 cm | MR Conditional | Available |
| 400SWSFT515-A | Length 15 cm | MR Conditional | Available |
FDA clearances
- 510(k) K230284 October 2023
Procedures that use coils
Frequently asked questions
What is swiftMATCH Coil, Soft 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 swiftMATCH Coil, Soft?
swiftMATCH Coil, Soft is made by Penumbra, Inc.. It is listed under embolization coils in our device library.
What sizes does swiftMATCH Coil, Soft come in?
Sizes listed for swiftMATCH Coil, Soft: Length: 6–15 cm. Confirm availability with the manufacturer's instructions for use.
Is swiftMATCH Coil, Soft MRI safe?
The FDA device database lists swiftMATCH Coil, Soft as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is swiftMATCH Coil, Soft FDA cleared?
swiftMATCH Coil, Soft is covered by FDA submission K230284.
How do I contact a Penumbra, Inc. sales representative?
Penumbra, Inc. has not listed representatives on LA Vascular yet. Visit the Penumbra, 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.