# K212988: ONO Retrieval Device

- Pathway: 510(k) (Traditional)
- Applicant: Onocor Vascular, LLC
- Decided: May 23, 2022 after 245 days
- Product code: MMX (Device, Percutaneous Retrieval)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K901502 (1990). 18 ancestors in all.
No later device cites it as a predicate yet.
2 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170987: Captus Vascular Retrieval System, Avantec Vascular Corporation (2017) Summary page 4.

## Indications for use
The Onocor ONO Retrieval device is indicated for use in the cardiovascular system to retrieve objects using minimally invasive surgical procedures. Procedures include retrieval of intravascular foreign objects such as coils, balloons, catheters, guidewires and/or filters within the cardiovascular system. This device is not intended for use in the coronary arteries or neurovasculature.

Source page: https://510kreport.com/device/K212988
Methodology: https://510kreport.com/methodology