# K211713: AngioCloud Service

- Pathway: 510(k) (Traditional)
- Applicant: Angiocloud, LLC
- Decided: Apr 28, 2022 after 329 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K954678 (1996). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171534: SurgicalPreview, Endo Vantage, LLC (2017) Summary page 4.

## Indications for use
The AngioCloud Service enables visualization and measurement of cerebral blood vessels for preoperational planning and sizing for neurovascular interventions and surgery. General functionalities are provided such as: * Segmentation of neurovascular structures * Centerline calculation * Visualization of 3D vascular images * Measurement and annotation tools * Case sharing and reporting tools Information provided by the software is not intended in any way to eliminate, replace, or substitute for, in whole or in part, the healthcare provider's judgment and analysis of the patient's condition.

Source page: https://510kreport.com/device/K211713
Methodology: https://510kreport.com/methodology