# K260938: Path BGC

- Pathway: 510(k) (Special)
- Applicant: Crossroads Neurovascular, Inc.
- Decided: Apr 15, 2026 after 26 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: 7 generations back to K010954 (2001). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242392: Path BGC, Crossroads Neurovascular, Inc. (2025) Summary page 5.

## 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/K260938
Methodology: https://510kreport.com/methodology