# Medical Devices; Neurological Devices; Classification of the Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment
> **Food and Drug Administration** · Final order. · Published 2016-12-23 · Effective 2016-12-23 · 81 FR 94251
## Document
- **Document number:** 2016-31007
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 81 FR 94251
- **CFR reference:** 21 CFR 882
- **Publication date:** 2016-12-23
- **Effective date:** 2016-12-23
- **HHS docket:** Docket No. FDA-2016-N-4165
## Abstract

The Food and Drug Administration (FDA) is classifying the neurovascular mechanical thrombectomy device for acute ischemic stroke treatment into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the neurovascular mechanical thrombectomy device for acute ischemic stroke treatment's classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2016/12/23/2016-31007/medical-devices-neurological-devices-classification-of-the-neurovascular-mechanical-thrombectomy)
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