Spinal Kinetics / Orthofix / Seaspine
Country not established
- Devices
- 1
What Spinal Kinetics / Orthofix / Seaspine makes
Spinal Kinetics, Orthofix, and Seaspine manufacture single-use, disposable spinal instrumentation, including the M6-C™ system designed for surgical procedures.
Their products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
M6-C™ Single Use, Disposable Instrumentation Ref K241117
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinal Kinetics / Orthofix / Seaspine have in the registry?
The registry currently lists 1 device for Spinal Kinetics / Orthofix / Seaspine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinal Kinetics / Orthofix / Seaspine's devices?
Among its 1 most recently registered device, Spinal Kinetics / Orthofix / Seaspine has devices listed in FDA 510(k) (1 device).
What risk classes do Spinal Kinetics / Orthofix / Seaspine's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spinal Kinetics / Orthofix / Seaspine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinal Kinetics / Orthofix / Seaspine in the registry?
The most recently registered devices listed for Spinal Kinetics / Orthofix / Seaspine include M6-C™ Single Use, Disposable Instrumentation.