Coils
Concerto Detachable 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.
Concerto Detachable 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 |
|---|---|---|---|
| NV-2-4-HELIX | — | MR Conditional | Available |
| NV-2-6-HELIX | — | MR Conditional | Available |
| NV-2-8-HELIX | — | MR Conditional | Available |
| NV-3-4-HELIX | — | MR Conditional | Available |
| NV-3-8-HELIX | — | MR Conditional | Available |
| NV-4-8-HELIX | — | MR Conditional | Available |
| NV-4-10-HELIX | — | MR Conditional | Available |
| NV-5-10-HELIX | — | MR Conditional | Available |
| NV-5-15-HELIX | — | MR Conditional | Available |
| NV-5-20-HELIX | — | MR Conditional | Available |
| NV-6-12-HELIX | — | MR Conditional | Available |
| NV-6-20-HELIX | — | MR Conditional | Available |
| NV-7-20-HELIX | — | MR Conditional | Available |
| NV-7-30-HELIX | — | MR Conditional | Available |
| NV-8-20-HELIX | — | MR Conditional | Available |
| NV-8-30-HELIX | — | MR Conditional | Available |
| NV-9-20-HELIX | — | MR Conditional | Available |
| NV-9-30-HELIX | — | MR Conditional | Available |
| NV-10-20-HELIX | — | MR Conditional | Available |
| NV-10-30-HELIX | — | MR Conditional | Available |
| PV-2-2-3D | — | MR Conditional | Available |
| PV-2-4-3D | — | MR Conditional | Available |
| PV-2-6-3D | — | MR Conditional | Available |
| PV-3-4-3D | — | MR Conditional | Available |
| PV-3-6-3D | — | MR Conditional | Available |
| PV-3-8-3D | — | MR Conditional | Available |
| PV-4-8-3D | — | MR Conditional | Available |
| PV-4-10-3D | — | MR Conditional | Available |
| PV-4-12-3D | — | MR Conditional | Available |
| PV-5-15-3D | — | MR Conditional | Available |
| PV-6-20-3D | — | MR Conditional | Available |
| PV-7-30-3D | — | MR Conditional | Available |
| PV-8-30-3D | — | MR Conditional | Available |
| PV-9-30-3D | — | MR Conditional | Available |
| PV-10-30-3D | — | MR Conditional | Available |
| PV-12-30-HELIX | — | MR Conditional | Available |
| PV-12-40-3D | — | MR Conditional | Available |
| PV-14-30-HELIX | — | MR Conditional | Available |
| PV-14-40-3D | — | MR Conditional | Available |
| PV-16-40-3D | — | MR Conditional | Available |
| PV-16-40-HELIX | — | MR Conditional | Available |
| PV-18-40-3D | — | MR Conditional | Available |
| PV-18-40-HELIX | — | MR Conditional | Available |
| PV-20-50-HELIX | — | MR Conditional | Available |
FDA clearances
- 510(k) K090046 February 2009
- 510(k) K081465 August 2008
Procedures that use coils
Frequently asked questions
What is Concerto Detachable 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 Concerto Detachable Coil System?
Concerto Detachable Coil System is made by Micro Therapeutics, Inc.. It is listed under embolization coils in our device library.
What sizes does Concerto Detachable Coil System come in?
The FDA device database does not list sizes for Concerto Detachable Coil System. Check the instructions for use or ask a Micro Therapeutics, Inc. representative.
Is Concerto Detachable Coil System MRI safe?
The FDA device database lists Concerto Detachable Coil System as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Concerto Detachable Coil System FDA cleared?
Concerto Detachable Coil System is covered by FDA submissions K090046, K081465.
How do I contact a Micro Therapeutics, Inc. sales representative?
Micro Therapeutics, Inc. has not listed representatives on LA Vascular yet. Visit the Micro Therapeutics, 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.