Deltaglide
Country not established
- Devices
- 1
What Deltaglide makes
Deltaglide manufactures the Tailwind, a medical device designed for spinal stabilization and fixation, intended for surgical use in orthopedic procedures.
The Tailwind is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Tailwind Ref K022704
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deltaglide have in the registry?
The registry currently lists 1 device for Deltaglide. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deltaglide's devices?
Among its 1 most recently registered device, Deltaglide has devices listed in FDA 510(k) (1 device).
What risk classes do Deltaglide's devices fall under?
Among its 1 most recently registered device, the classes recorded for Deltaglide's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deltaglide in the registry?
The most recently registered devices listed for Deltaglide include TAILWIND.