Medtronic Soafamor Danek
Country not established
- Devices
- 1
What Medtronic Soafamor Danek makes
Medtronic Soafamor Danek manufactures spinal reconstruction systems, including the VERTEX RECONSTRUCTION SYSTEM and VERTEX SELECT RECONSTRUCTION SYSTEM, designed for surgical applications in spinal stabilization and fixation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Soafamor Danek have in the registry?
The registry currently lists 1 device for Medtronic Soafamor Danek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Soafamor Danek's devices?
Among its 1 most recently registered device, Medtronic Soafamor Danek has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Soafamor Danek's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Soafamor Danek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Soafamor Danek in the registry?
The most recently registered devices listed for Medtronic Soafamor Danek include VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM.