Jg Spine, LLC
Country not established
- Devices
- 1
What Jg Spine, LLC makes
Jg Spine, LLC manufactures the SUREFIX Interspinous Fusion System, a device designed for spinal stabilization by promoting fusion between adjacent vertebrae.
The SUREFIX Interspinous Fusion System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Surefix Interspinous Fusion System Ref K124014
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jg Spine, LLC have in the registry?
The registry currently lists 1 device for Jg Spine, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jg Spine, LLC's devices?
Among its 1 most recently registered device, Jg Spine, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Jg Spine, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jg Spine, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jg Spine, LLC in the registry?
The most recently registered devices listed for Jg Spine, LLC include SUREFIX INTERSPINOUS FUSION SYSTEM.