Corespine Technologies, LLC
Country not established
- Devices
- 1
What Corespine Technologies, LLC makes
Corespine Technologies, LLC makes the XTEND-ST Nucleus Removal System, Model 9004, a device used for removing nucleus pulposus material during spinal procedures.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Xtend-St Nucleus Removal System, Model 9004 Ref K090303
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corespine Technologies, LLC have in the registry?
The registry currently lists 1 device for Corespine Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corespine Technologies, LLC's devices?
Among its 1 most recently registered device, Corespine Technologies, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Corespine Technologies, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Corespine Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corespine Technologies, LLC in the registry?
The most recently registered devices listed for Corespine Technologies, LLC include XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004.