Osteocentric Trauma
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
OsteoCentric Bone Plate and Screw System Ref K190430
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteocentric Trauma have in the registry?
The registry currently lists 1 device for Osteocentric Trauma. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteocentric Trauma's devices?
Among its 1 most recently registered device, Osteocentric Trauma has devices listed in FDA 510(k) (1 device).
What risk classes do Osteocentric Trauma's devices fall under?
Among its 1 most recently registered device, the classes recorded for Osteocentric Trauma's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteocentric Trauma in the registry?
The most recently registered devices listed for Osteocentric Trauma include OsteoCentric Bone Plate and Screw System.