Powerbasetec GmbH
GermanyFDA applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Powerbasetec GmbH makes
Powerbasetec GmbH manufactures the ParaMotion, a medical device designed for spinal stabilization and motion preservation, intended to assist in surgical interventions for spinal conditions.
The ParaMotion is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
ParaMotion Ref K203761
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Powerbase Tec GmbH Gieboldehausen, Niedersachsen Lower Saxony · DE FEI 3022115583
Frequently asked questions
How many devices does Powerbasetec GmbH have in the registry?
The registry currently lists 1 device for Powerbasetec GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Powerbasetec GmbH's devices?
Among its 1 most recently registered device, Powerbasetec GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Powerbasetec GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Powerbasetec GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Powerbasetec GmbH in the registry?
The most recently registered devices listed for Powerbasetec GmbH include ParaMotion.
Which FDA establishments are linked to Powerbasetec GmbH?
1 FDA establishment is linked to Powerbasetec GmbH in the registry; they are listed on the company page.