# K261772: Target Xtra Detachable Coil

- Pathway: 510(k) (Special)
- Applicant: Stryker Neurovscular
- Decided: Jun 24, 2026 after 26 days
- Product code: HCG (Device, Neurovascular Embolization)
- Device class: 2
- Regulation: 21 CFR 882.5950
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 17 generations back to K951256 (1995). 43 ancestors in all.
No later device cites it as a predicate yet.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K252694: Target Detachable Coil, Stryker Neurovascular (2025) Summary page 5.

## Indications for use
Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. Target Detachable Coils are indicated for endovascular embolization of: * Intracranial aneurysms » Other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae Arterial and venous embolizations in the peripheral vasculature

Source page: https://510kreport.com/device/K261772
Methodology: https://510kreport.com/methodology