Camber Spine
Country not established
- Devices
- 4
What Camber Spine makes
Camber Spine manufactures spinal interbody fusion cages, including the VERTA Corpectomy Cage for lumbar applications, the COVERIS Cervical Cage for cervical spine procedures, and the DIAGON Oblique Cage for lateral access surgeries. The company also produces the ORTHROS Posterior Stabilization System, designed for posterior spinal fixation and support.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.
Catalogue
VERTA Corpectomy Cage Ref K143490
Regimes: 510(k) Registry: 510(k)Camber Spine Coveris Cervical Cage Ref K133529
Regimes: 510(k) Registry: 510(k)Camber Spine Diagon Oblique Cage Ref K134038
Regimes: 510(k) Registry: 510(k)Orthros Posterior Stabilization System Ref K133366
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Camber Spine have in the registry?
The registry currently lists 4 devices for Camber Spine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Camber Spine's devices?
Among its 4 most recently registered devices, Camber Spine has devices listed in FDA 510(k) (4 devices).
What risk classes do Camber Spine's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Camber Spine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Camber Spine in the registry?
The most recently registered devices listed for Camber Spine include VERTA Corpectomy Cage, CAMBER SPINE COVERIS CERVICAL CAGE, CAMBER SPINE DIAGON OBLIQUE CAGE and ORTHROS POSTERIOR STABILIZATION SYSTEM.