# K130649: Silk Road Access Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Silk Road Medical, Inc.
- Decided: Nov 1, 2013 after 235 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K010954 (2001). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070970: Neuron Support Catheter System, Model 5F/6F, Penumbra, Inc. (2007) Summary page 2.
- K082290: Neuron Delivery Catheter 070, Penumbra, Inc. (2008) Summary page 2.

## Most influential descendants
- K143459: Silk Road Acccess Catheter (2015), 0 descendants of its own

## Indications for use
The Silk Road TM Access, Catheter is indicated for the introduction of interventional devices into the peripheral vasculature.

Source page: https://510kreport.com/device/K130649
Methodology: https://510kreport.com/methodology