# K253511: Concerto Versa™ Detachable Coil

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic, Inc.
- Decided: Jan 14, 2026 after 70 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: 14 generations back to K951256 (1995). 62 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K202850: Concerto Versa, Detachable Coil, Micro Therapeutics, Inc. d/b/a ev3 Neurovascular (2021) Summary page 5.

## Most influential descendants
- K261866: Concerto Versa™ Detachable Coil (2026), 0 descendants of its own

## 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/K253511
Methodology: https://510kreport.com/methodology