Konigsee Implantate GmbH
Country not established
- Devices
- 1
What Konigsee Implantate GmbH makes
Konigsee Implantate GmbH manufactures the SFC Vertebral Body Replacement, a spinal implant designed for vertebral body replacement procedures.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Sfc Vertebral Body Replacement Ref K110153
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Konigsee Implantate GmbH have in the registry?
The registry currently lists 1 device for Konigsee Implantate GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Konigsee Implantate GmbH's devices?
Among its 1 most recently registered device, Konigsee Implantate GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Konigsee Implantate GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Konigsee Implantate GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Konigsee Implantate GmbH in the registry?
The most recently registered devices listed for Konigsee Implantate GmbH include SFC VERTEBRAL BODY REPLACEMENT.