# K211120: ERIC Retrieval Device

- Pathway: 510(k) (Traditional)
- Applicant: MicroVention, Inc.
- Decided: Mar 31, 2022 after 350 days
- Product code: NRY (Catheter, Thrombus Retriever)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K003410 (2001). 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)
- K143077: Trevo XP ProVue Retriever (6X25mm), Concentric Medical, Inc. (2015) Summary page 4.
- K150616: Trevo XP ProVue Retriever (4x30mm), Concentric Medical, Inc. (2015) Summary page 4.
- K132641: Modified Trevo Provue Retriever, Concentric Medical, Inc. (2014) Summary page 4.

## Recalls of this device
- Aug 5, 2024 · Class II · Z-3157-2024: Due to Retrieval Device product labels stating the incorrect expiration dates that (5 years instead of 3 years) which extends beyond their true expiration date.

## Indications for use
The ERIC Retrieval Device is indicated to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment.

Source page: https://510kreport.com/device/K211120
Methodology: https://510kreport.com/methodology