# K242392: Path BGC

- Pathway: 510(k) (Traditional)
- Applicant: Crossroads Neurovascular, Inc.
- Decided: May 9, 2025 after 270 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- 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: 6 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)
- K131492: Modified Flowgate Balloon Guide Catheter, Concentric Medical, Inc. (2013) Summary page 5.

## Most influential descendants
- K260938: Path BGC (2026), 0 descendants of its own

## Indications for use
PATH BGC is indicated for use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the neurovascular system. The balloon provides temporary vascular occlusion during these and other angiographic procedures.

Source page: https://510kreport.com/device/K242392
Methodology: https://510kreport.com/methodology