# K102912: Interlock Fibered Idc Occlusion System

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific
- Decided: Mar 3, 2011 after 153 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 K060078 (2006). 1 ancestor in all.
4 later devices descend 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)
- K060078: Fibered Idc Occlusion System, Boston Scientific Corporation (2006) Summary page 1.

## Most influential descendants
- K132578: Interlock - 18 Fibered Idc Occlusion System (2013), 3 descendants of its own
- K213398: EMBOLD Fibered Detachable Coil System (2022), 1 descendant of its own
- K250276: Nitinol Enhanced Device (NED) (2025), 0 descendants of its own
- K230706: EMBOLD™ Soft Detachable Coil System (2023), 0 descendants of its own

## Indications for use
The Interlock™ Fibered IDC™ Occlusion System is a modified interlocking detachable coil indicated 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/K102912
Methodology: https://510kreport.com/methodology