Allure Spine LLC
Country not established
- Devices
- 1
What Allure Spine LLC makes
Allure Spine LLC manufactures the Spondy Spinal Fixation System, a device designed for internal spinal stabilization and fusion procedures.
The Spondy Spinal Fixation System is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Spondy Spinal Fixation System Ref K100956
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allure Spine LLC have in the registry?
The registry currently lists 1 device for Allure Spine LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allure Spine LLC's devices?
Among its 1 most recently registered device, Allure Spine LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Allure Spine LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Allure Spine LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Allure Spine LLC in the registry?
The most recently registered devices listed for Allure Spine LLC include SPONDY SPINAL FIXATION SYSTEM.