Medtronic Spinal and Biologics Div
Country not established
- Devices
- 1
What Medtronic Spinal and Biologics Div makes
The company designs modifications to the Verte-Stack spinal system, a device used for spinal stabilization procedures.
These products are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Modification To Verte-Stack Spinal System Ref K062133
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Spinal and Biologics Div have in the registry?
The registry currently lists 1 device for Medtronic Spinal and Biologics Div. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Spinal and Biologics Div's devices?
Among its 1 most recently registered device, Medtronic Spinal and Biologics Div has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Spinal and Biologics Div's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Spinal and Biologics Div's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Spinal and Biologics Div in the registry?
The most recently registered devices listed for Medtronic Spinal and Biologics Div include MODIFICATION TO VERTE-STACK SPINAL SYSTEM.