# K120850: Target Detachable Coil

- Pathway: 510(k) (Special)
- Applicant: Stryker Neurovascular
- Decided: Apr 17, 2012 after 27 days
- Product code: HCG (Device, Neurovascular Embolization)
- Device class: 2
- Regulation: 21 CFR 882.5950
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K951256 (1995). 36 ancestors in all.
No later device cites it as a predicate yet.
0 of 37 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093142: Target Detachable Coils and Inzone Detachment System, Boston Scientific Corp (2010) Summary page 2.
- K102672: Target Detachable Coil, Boston Scientific Corp (2010) Summary page 2.
- K112385: Traget Detachable Coil, Stryker Neurovascular (2011) Summary page 5.

## Recalls of this device
- Oct 22, 2014 · Class II · Z-0481-2015: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were shipped to US customers beyond the expiration date.

## Indications for use
Target Detachable Coils are indicated for the 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/K120850
Methodology: https://510kreport.com/methodology