Torrey Spine
Country not established
- Devices
- 1
What Torrey Spine makes
Torrey Spine manufactures the Viceroy Spinal System, a Class II spinal implant designed for surgical fixation in the spine, intended to stabilize vertebrae and promote proper alignment during healing.
The Viceroy Spinal System is regulated under FDA 510(k) clearance as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Viceroy Spinal System Ref K122229
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Torrey Spine have in the registry?
The registry currently lists 1 device for Torrey Spine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Torrey Spine's devices?
Among its 1 most recently registered device, Torrey Spine has devices listed in FDA 510(k) (1 device).
What risk classes do Torrey Spine's devices fall under?
Among its 1 most recently registered device, the classes recorded for Torrey Spine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Torrey Spine in the registry?
The most recently registered devices listed for Torrey Spine include VICEROY SPINAL SYSTEM.