Arthro-Dif
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Acrosspine Pedicle Screw System Ref K141695
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthro-Dif have in the registry?
The registry currently lists 1 device for Arthro-Dif. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthro-Dif's devices?
Among its 1 most recently registered device, Arthro-Dif has devices listed in FDA 510(k) (1 device).
What risk classes do Arthro-Dif's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arthro-Dif's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthro-Dif in the registry?
The most recently registered devices listed for Arthro-Dif include ACROSSPINE PEDICLE SCREW SYSTEM.