Spinal Edge, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Spinal Edge, LLC makes
Spinal Edge, LLC manufactures spinal implants and fixation hardware, including the Atlas spinal cage and intervertebral body cage. The company also produces the Titan pedicle screw system.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) regulatory registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Atlas Intervertebral Body Cage Ref K092774
Regimes: 510(k) Registry: 510(k)Spinal Edge Titan Pedicle Screw System Ref K091110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinal Edge, LLC have in the registry?
The registry currently lists 3 devices for Spinal Edge, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinal Edge, LLC's devices?
Among its 3 most recently registered devices, Spinal Edge, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Spinal Edge, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Spinal Edge, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinal Edge, LLC in the registry?
The most recently registered devices listed for Spinal Edge, LLC include ATLAS SPINAL CAGE, MODELS SC-150-007, 009, 011, 013, 015, 017., ATLAS INTERVERTEBRAL BODY CAGE and SPINAL EDGE TITAN PEDICLE SCREW SYSTEM.