# K112385: Traget Detachable Coil

- Pathway: 510(k) (Special)
- Applicant: Stryker Neurovascular
- Decided: Sep 15, 2011 after 28 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: 9 generations back to K951256 (1995). 35 ancestors in all.
15 later devices descend from it; 3 cite it directly.
0 of 51 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.

## Most influential descendants
- K113412: Target Detachable Coil (2011), 13 descendants of its own
- K123377: Target Detachable Coil (2012), 12 descendants of its own
- K153658: Target Detachable Coils (2016), 11 descendants of its own
- K161429: Target Detachable Coils (2016), 10 descendants of its own
- K222533: Target Tetra Detachable Coils (2022), 3 descendants of its own

## 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/K112385
Methodology: https://510kreport.com/methodology