Spinemed Ges.M.B.H
AustriaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
ACRON™ TLIF System Ref K171151
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinemed Ges.M.B.H have in the registry?
The registry currently lists 1 device for Spinemed Ges.M.B.H. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinemed Ges.M.B.H's devices?
Among its 1 most recently registered device, Spinemed Ges.M.B.H has devices listed in FDA 510(k) (1 device).
What risk classes do Spinemed Ges.M.B.H's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spinemed Ges.M.B.H's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinemed Ges.M.B.H in the registry?
The most recently registered devices listed for Spinemed Ges.M.B.H include ACRON™ TLIF System.