# K060078: Fibered Idc Occlusion System

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corporation
- Decided: Jan 31, 2006 after 21 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
No predicates in its family tree.
9 later devices descend from it; 3 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Interlocking Detachable Coil System (IDC System): named in the summary without a submission number
- (no number) Guglielmi Detachable Coil (GDC): named in the summary without a submission number
- (no number) GDC VortX: named in the summary without a submission number
- (no number) VortX-18 Pushable Coils: named in the summary without a submission number
- (no number) VortX-18 Diamond Pushable Coils: named in the summary without a submission number

## Most influential descendants
- K102912: Interlock Fibered Idc Occlusion System (2011), 4 descendants of its own
- K132578: Interlock - 18 Fibered Idc Occlusion System (2013), 3 descendants of its own
- K110295: Interlock-35 Fibered Idc Occlusion System (2011), 3 descendants of its own
- K112103: Interlock-35 Fibered Idc Occlusion System (2011), 2 descendants of its own
- K213398: EMBOLD Fibered Detachable Coil System (2022), 1 descendant of its own

## Indications for use
The 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/K060078
Methodology: https://510kreport.com/methodology