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.
FDA clearances
- 510(k) K253511 January 2026
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 Medtronic, 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 Medtronic, 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 K253511.
How do I contact a Medtronic, Inc. sales representative?
Medtronic, Inc. has not listed representatives on LA Vascular yet. Visit the Medtronic, 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.