# K133208: Interlock-35 Fibered Idc Occlusion System

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corp
- Decided: Nov 14, 2013 after 27 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: 4 generations back to K955293 (1996). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113651: Interlock-35 Fibered Idc Occlusion System, Boston Scientific Corporation (2012) Summary page 1.

## Indications for use
The lnterlock-35 Fibered IDO Occlusion System is indicated for obstructing or reducing blood flow in the peripheral vasculature during embolizalion procedures. This device Is not intended for neurovascular use.

Source page: https://510kreport.com/device/K133208
Methodology: https://510kreport.com/methodology