Creaspine
Country not established
- Devices
- 3
What Creaspine makes
Creaspine manufactures vertebral body replacement systems, including the Creaspine Supstance Vertebral Body Replacement System Line Extension and the Creaspine Supstance Small Vertebral Body Replacement System, which are implantable devices used for spinal reconstruction.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. Creaspine is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Creaspine have in the registry?
The registry currently lists 3 devices for Creaspine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Creaspine's devices?
Among its 3 most recently registered devices, Creaspine has devices listed in FDA 510(k) (3 devices).
What risk classes do Creaspine's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Creaspine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Creaspine in the registry?
The most recently registered devices listed for Creaspine include CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM, CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM LINE EXTENSION and CREASPINE SUPSTANCE SMALL VERTEBRAL BODY REPLACEMENT SYSTEM.