Otto Bock Austria
Country not established
- Devices
- 2
What Otto Bock Austria makes
Otto Bock Austria manufactures the AXON-BUS prosthetic system, a modular lower-limb prosthetic solution designed for improved mobility and functionality in amputees. The system integrates advanced control interfaces and mechanical components to support active movement and weight-bearing activities.
The AXON-BUS prosthetic system is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Stiwell MED4 Ref K080950
Regimes: 510(k) Registry: 510(k)Axon-Bus Prosthetic System Ref K123795
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Otto Bock Austria have in the registry?
The registry currently lists 2 devices for Otto Bock Austria. Devices recorded under merged duplicate company entries are counted once.
Which registries list Otto Bock Austria's devices?
Among its 2 most recently registered devices, Otto Bock Austria has devices listed in FDA 510(k) (2 devices).
What risk classes do Otto Bock Austria's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Otto Bock Austria's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Otto Bock Austria in the registry?
The most recently registered devices listed for Otto Bock Austria include STIWELL MED4 and AXON-BUS PROSTHETIC SYSTEM.