Medical Device Advisory Development Group
Country not established
- Devices
- 1
What Medical Device Advisory Development Group makes
The company designs and manufactures the Selective-Axis Posterior Noncervical Plating System, a surgical implant used for spinal stabilization in noncervical regions. This device is intended for internal fixation of vertebral bodies, providing structural support during spinal fusion procedures.
The Selective-Axis Posterior Noncervical Plating System is classified as a Class II medical device in the US and is subject to 510(k) clearance through the FDA. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Device Advisory Development Group have in the registry?
The registry currently lists 1 device for Medical Device Advisory Development Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Device Advisory Development Group's devices?
Among its 1 most recently registered device, Medical Device Advisory Development Group has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Device Advisory Development Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Device Advisory Development Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Device Advisory Development Group in the registry?
The most recently registered devices listed for Medical Device Advisory Development Group include SELECTIVE-AXIS POSTERIOR NONCERVICAL PLATING SYSTEM.