Medtronic Neurovascular
Country not established
- Devices
- 1
What Medtronic Neurovascular makes
Medtronic Neurovascular designs and manufactures revascularization devices, including the Solitaire 2 and Solitaire Platinum, which are intended for mechanical thrombectomy in stroke patients to restore blood flow in occluded cerebral arteries.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Neurovascular have in the registry?
The registry currently lists 1 device for Medtronic Neurovascular. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Neurovascular's devices?
Among its 1 most recently registered device, Medtronic Neurovascular has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Neurovascular's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Neurovascular's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Neurovascular in the registry?
The most recently registered devices listed for Medtronic Neurovascular include Solitaire 2 and Solitaire Platinum Revascularization Device.