# K213494: Aveir Retrieval Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Abbott Medical
- Decided: Apr 1, 2022 after 151 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: 7 generations back to K901502 (1990). 17 ancestors in all.
No later device cites it as a predicate yet.
1 of 18 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092343: EN Snare Endovascular Snare System, Merit Medical Systems, Inc. (2009) Summary page 5.
- K122088: Merit One Snare System, Merit Medical Systems, Inc. (2012) Summary page 5.
- K133681: Crux Snare Filter Retrieval Set, Volcano Corporation (2014) Summary page 5.

## Indications for use
The Aveir Retrieval Catheter is intended to be used in the peripheral vasculature and the cardiovascular system to retrieve and manipulate an Abbott Medical leadless pacemaker (LP). Retrieval and manipulation includes removing the LP from the heart or peripheral vasculature.

Source page: https://510kreport.com/device/K213494
Methodology: https://510kreport.com/methodology