Coils
Concerto Versa
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 Versa 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 |
|---|---|---|---|
| CV-3-5 | — | MR Conditional | Available |
| CV-3-15 | — | MR Conditional | Available |
| CV-4-5 | — | MR Conditional | Available |
| CV-4-15 | — | MR Conditional | Available |
| CV-5-20 | — | MR Conditional | Available |
| CV-5-30 | — | MR Conditional | Available |
| CV-6-20 | — | MR Conditional | Available |
| CV-6-40 | — | MR Conditional | Available |
| CV-7-20 | — | MR Conditional | Available |
| CV-7-40 | — | MR Conditional | Available |
| CV-8-20 | — | MR Conditional | Available |
| CV-8-40 | — | MR Conditional | Available |
| CV-9-20 | — | MR Conditional | Available |
| CV-9-40 | — | MR Conditional | Available |
| CV-10-20 | — | MR Conditional | Available |
| CV-10-40 | — | MR Conditional | Available |
| CV-12-30 | — | MR Conditional | Available |
| CV-12-50 | — | MR Conditional | Available |
| CV-14-40 | — | MR Conditional | Available |
| CV-14-65 | — | MR Conditional | Available |
| CV-16-40 | — | MR Conditional | Available |
| CV-16-65 | — | MR Conditional | Available |
| CV-18-40 | — | MR Conditional | Available |
| CV-18-65 | — | MR Conditional | Available |
| CV-20-40 | — | MR Conditional | Available |
| CV-20-65 | — | MR Conditional | Available |
| CV-24-40 | — | MR Conditional | Available |
| CV-24-65 | — | MR Conditional | Available |
| CV-28-40 | — | MR Conditional | Available |
| CV-28-65 | — | MR Conditional | Available |
| CV-32-40 | — | MR Conditional | Available |
| CV-32-65 | — | MR Conditional | Available |
FDA clearances
- 510(k) K202850 February 2021
Procedures that use coils
Frequently asked questions
What is Concerto Versa 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 Versa?
Concerto Versa is made by Micro Therapeutics, Inc.. It is listed under embolization coils in our device library.
What sizes does Concerto Versa come in?
The FDA device database does not list sizes for Concerto Versa. Check the instructions for use or ask a Micro Therapeutics, Inc. representative.
Is Concerto Versa MRI safe?
The FDA device database lists Concerto Versa as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Concerto Versa FDA cleared?
Concerto Versa is covered by FDA submission K202850.
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.