# K122735: Sorin Vasculoop Two Tie Endoscopic Ligation System Model DTTS2

- Pathway: 510(k) (Traditional)
- Applicant: Sorin Group USA, Inc.
- Decided: May 21, 2013 after 257 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- 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 K925914 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925914: Pre-Tied Loop Suture Cannula, ETHICON, Inc. (1993) Summary page 1.

## Indications for use
the Sorin VascuLoop is used for proximal and distal ligation of vessels during endoscopic vessel harvesting procedures.

Source page: https://510kreport.com/device/K122735
Methodology: https://510kreport.com/methodology