# K091952: Acta Vessel Occlusion System (Vos)

- Pathway: 510(k) (Abbreviated)
- Applicant: Nfocus Neuromedical, Inc.
- Decided: Sep 10, 2010 after 436 days
- Product code: KRD (Device, Vascular, For Promoting Embolization)
- Device class: 2
- Regulation: 21 CFR 870.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Amplatzer Vascular plug: named in the summary without a submission number

## Indications for use
The Nfocus Neuromedical Acta Vessel Occlusion System (VOS) is indicated for arterial and venous embolizations in the peripheral vasculature specifically within the abdominal and thoracic cavities.

Source page: https://510kreport.com/device/K091952
Methodology: https://510kreport.com/methodology