# K002181: GDC Ultrasoft Coil

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific, Target
- Decided: Aug 11, 2000 after 23 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
No predicates in its family tree.
60 later devices descend from it; 2 cite it directly.
0 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K093142: Target Detachable Coils and Inzone Detachment System (2010), 58 descendants of its own
- K103008: Inzone Detachment System (2010), 21 descendants of its own
- K102672: Target Detachable Coil (2010), 16 descendants of its own
- K123338: Barricade Embolization Coil System (2013), 15 descendants of its own
- K112385: Traget Detachable Coil (2011), 15 descendants of its own

Source page: https://510kreport.com/device/K002181
Methodology: https://510kreport.com/methodology