Vitalitec Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Vitalitec Medizintechnik GmbH makes
Vitalitec Medizintechnik GmbH manufactures Kerrison Rongeurs, which are surgical instruments used for bone removal during spinal and neurosurgical procedures.
The company's products are listed in the FDA 510(k) registry and are classified as Class II medical devices. Vitalitec Medizintechnik GmbH is based in the US.
Catalogue
Kerrison Rongeurs Ref K152734
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vitalitec Medizintechnik GmbH have in the registry?
The registry currently lists 1 device for Vitalitec Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitalitec Medizintechnik GmbH's devices?
Among its 1 most recently registered device, Vitalitec Medizintechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Vitalitec Medizintechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitalitec Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitalitec Medizintechnik GmbH in the registry?
The most recently registered devices listed for Vitalitec Medizintechnik GmbH include Kerrison Rongeurs.