510(k) Report

FDA product code · Neurology

Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment

POLClass II21 CFR 882.5600510(k) required18 decisions since 20161 recall

18 FDA decisions since 2016. 510(k) reviews decided 2021–2025 took a median of 149 days (half between 127 and 170). 1 recall names this code; it is Class I. The most-cited predicate is K162539, named by 4 later devices.

A neurovascular mechanical thrombectomy device for acute ischemic stroke treatment is a prescription device used in the treatment of acute ischemic stroke to improve clinical outcomes. The device is delivered into the neurovasculature with an endovascular approach, mechanically removes thrombus from the body, and restores blood flow in the neurovasculature.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, neurology panel

Twenty years of POL at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · POL

1in 2025

2016: 22018: 32019: 42020: 32021: 22023: 32025: 1
2007high 4 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · POL

144in 2023

2018: 123 days median2019: 95 days median2020: 57 days median2023: 144 days median
2007high 144 (2023) · low 57 (2020)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · POL

1in 2020

2020: 1, 1 Class I
2007high 1 (2020) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · POL

16in 2025

2019: 12020: 62021: 212022: 102023: 232024: 112025: 16
2007high 23 (2023) · low 0 (2007)2025

MAUDE reports naming product code POL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20162—00
20170—00
2018312300
201949501
20203571 (1)6
20212—021
20220—010
20233144023
20240—011
20251—016
20260—0—
FIG. 1 — POL by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in POL? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report