Spinepoint, LLC
Country not established
- Devices
- 1
What Spinepoint, LLC makes
Spinepoint, LLC manufactures the Flex-Z™ Cervical Cage, a spinal interbody device designed for anterior cervical discectomy and fusion procedures. This product is intended to provide structural support and promote spinal stability in the cervical spine region.
The Flex-Z™ Cervical Cage is classified as a Class II medical device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States.
Catalogue
Flex-Z™ Cervical Cage Ref K252432
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinepoint, LLC have in the registry?
The registry currently lists 1 device for Spinepoint, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinepoint, LLC's devices?
Among its 1 most recently registered device, Spinepoint, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Spinepoint, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spinepoint, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinepoint, LLC in the registry?
The most recently registered devices listed for Spinepoint, LLC include Flex-Z™ Cervical Cage.