# K040342: Interlocking Detachable Coil System (Idc)

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Apr 13, 2004 after 61 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: 1 generation back to K891688 (1989). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K911779: Helix Shaped Coils with Dacron Fibers, Modified, Target Therapeutics (1991) Summary page 1.
- K914786: Target Therapeutics Coils, Target Therapeutics (1992) Summary page 1.
- K891688: Coil and Coil Delivery System, Target Therapeutics (1989) Summary page 1.
- K901721: Modified Target Therapeutics Coils, Target Therapeutics (1990) Summary page 1.

## Most influential descendants
- K141378: Idc Interlocking Detachable Coil (2014), 0 descendants of its own

## Indications for use
The IDC System is indited to obstruct or reduce rate of blood flow in the peripheral vasculature. This device is not intended for neurovascular use.

Source page: https://510kreport.com/device/K040342
Methodology: https://510kreport.com/methodology