# K261866: Concerto Versa™ Detachable Coil

- Pathway: 510(k) (Special)
- Applicant: Medtronic, Inc.
- Decided: Jun 24, 2026 after 20 days
- Product code: KRD (Device, Vascular, For Promoting Embolization)
- Device class: 2
- Regulation: 21 CFR 870.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 15 generations back to K951256 (1995). 63 ancestors in all.
No later device cites it as a predicate yet.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K253511: Concerto Versa™ Detachable Coil, Medtronic, Inc. (2026) Summary page 5.

## Indications for use
The Concerto Versa™ Detachable Coil is indicated for arterial and venous embolization in the peripheral vasculature.

Source page: https://510kreport.com/device/K261866
Methodology: https://510kreport.com/methodology