Coils
Swift Coil System
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.
Swift Coil 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 |
|---|---|---|---|
| 400SWCCL102-A | Length 2 cm | MR Conditional | Available |
| 400SWCCL103-A | Length 3 cm | MR Conditional | Available |
| 400SWCCL105-A | Length 5 cm | MR Conditional | Available |
| 400SWCCL202-A | Length 2 cm | MR Conditional | Available |
| 400SWCCL204-A | Length 4 cm | MR Conditional | Available |
| 400SWCCL210-A | Length 10 cm | MR Conditional | Available |
| 400SWCCL306-A | Length 6 cm | MR Conditional | Available |
| 400SWCCL310-A | Length 10 cm | MR Conditional | Available |
| 400SWCCL408-A | Length 8 cm | MR Conditional | Available |
| 400SWCCL410-A | Length 10 cm | MR Conditional | Available |
| 400SWCCL430-A | Length 30 cm | MR Conditional | Available |
| 400SWCCL510-A | Length 10 cm | MR Conditional | Available |
| 400SWCCL512-A | Length 12 cm | MR Conditional | Available |
| 400SWCCL530-A | Length 30 cm | MR Conditional | Available |
| 400SWPC01-A | Length 1 cm | MR Conditional | Available |
| 400SWPC02-A | Length 2 cm | MR Conditional | Available |
| 400SWPC03-A | Length 3 cm | MR Conditional | Available |
| 400SWPC04-A | Length 4 cm | MR Conditional | Available |
| 400SWPC05-A | Length 5 cm | MR Conditional | Available |
| 400SWPC06-A | Length 6 cm | MR Conditional | Available |
| 400SWPC07-A | Length 7 cm | MR Conditional | Available |
| 400SWPC08-A | Length 8 cm | MR Conditional | Available |
| 400SWPC09-A | Length 9 cm | MR Conditional | Available |
| 400SWPC10-A | Length 10 cm | MR Conditional | Available |
| 400SWPC12-A | Length 12 cm | MR Conditional | Available |
| 400SWPC15-A | Length 15 cm | MR Conditional | Available |
| 400SWPC20-A | Length 20 cm | MR Conditional | Available |
| 400SWPC25-A | Length 25 cm | MR Conditional | Available |
| 400SWPC30-A | Length 30 cm | MR Conditional | Available |
| 400SWPC35-A | Length 35 cm | MR Conditional | Available |
| 400SWPC40-A | Length 40 cm | MR Conditional | Available |
| 400SWPC45-A | Length 45 cm | MR Conditional | Available |
| 400SWPC50-A | Length 50 cm | MR Conditional | Available |
| 400SWPC55-A | Length 55 cm | MR Conditional | Available |
| 400SWPC60-A | Length 60 cm | MR Conditional | Available |
| SDH1-A | — | MR Unsafe | Available |
FDA clearances
- 510(k) K230284 October 2023
Procedures that use coils
Frequently asked questions
What is Swift Coil System 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 Swift Coil System?
Swift Coil System is made by Penumbra, Inc.. It is listed under embolization coils in our device library.
What sizes does Swift Coil System come in?
Sizes listed for Swift Coil System: Length: 1–60 cm. Confirm availability with the manufacturer's instructions for use.
Is Swift Coil System MRI safe?
The FDA device database lists Swift Coil System as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Swift Coil System FDA cleared?
Swift Coil System 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.