Coorstek Medical
Country not established
- Devices
- 1
What Coorstek Medical makes
Coorstek Medical makes the Integrity-SI TM Fusion System, which is a spinal fusion device used in orthopedic surgery.
The Integrity-SI TM Fusion System is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Integrity-SI TM Fusion System Ref K161755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coorstek Medical have in the registry?
The registry currently lists 1 device for Coorstek Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coorstek Medical's devices?
Among its 1 most recently registered device, Coorstek Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Coorstek Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Coorstek Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coorstek Medical in the registry?
The most recently registered devices listed for Coorstek Medical include Integrity-SI TM Fusion System.