Spine360
Country not established
- Devices
- 2
What Spine360 makes
Spine360 manufactures spinal hardware, specifically the Anterior Cervical Plate System and the Talon Spinal System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
SPINE360 Anterior Cervical Plate System Ref K092531
Regimes: 510(k) Registry: 510(k)Talon Spinal System Ref K102995
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spine360 have in the registry?
The registry currently lists 2 devices for Spine360. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spine360's devices?
Among its 2 most recently registered devices, Spine360 has devices listed in FDA 510(k) (2 devices).
What risk classes do Spine360's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Spine360's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spine360 in the registry?
The most recently registered devices listed for Spine360 include SPINE360 ANTERIOR CERVICAL PLATE SYSTEM and TALON SPINAL SYSTEM.