Navier Medical
AustraliaFDA applicant, unverified
- Devices
- 1
What Navier Medical makes
Navier Medical produces the Mosaic device, a Class II medical device designed for vascular applications, including stent graft systems for endovascular aneurysm repair (EVAR) and peripheral vascular interventions.
The Mosaic device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Mosaic (V1.0.1) Ref K244012
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Navier Medical have in the registry?
The registry currently lists 1 device for Navier Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Navier Medical's devices?
Among its 1 most recently registered device, Navier Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Navier Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Navier Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Navier Medical in the registry?
The most recently registered devices listed for Navier Medical include Mosaic (V1.0.1).