Peripheral Ave
Country not established
- Devices
- 2
What Peripheral Ave makes
Peripheral Ave manufactures the Peripheral Ave Stent System, a vascular stent designed for peripheral artery applications, and the Medtronic Ave Stent Delivery System, which is intended for biliary tract procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Peripheral Ave Stent System Ref K983008
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peripheral Ave have in the registry?
The registry currently lists 2 devices for Peripheral Ave. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peripheral Ave's devices?
Among its 2 most recently registered devices, Peripheral Ave has devices listed in FDA 510(k) (2 devices).
What risk classes do Peripheral Ave's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Peripheral Ave's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peripheral Ave in the registry?
The most recently registered devices listed for Peripheral Ave include PERIPHERAL AVE STENT SYSTEM and MEDTRONIC AVE STENT DELIVERY SYSTEM - FOR USE IN BILIARY INDICATION.