The Skeletal Design Partnership, Ltd.
Country not established
- Devices
- 1
What The Skeletal Design Partnership, Ltd. makes
The Skeletal Design Partnership, Ltd. manufactures the Foundation Spinal System, which is a spinal fixation device.
This device is classified as Class II and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Foundation Spinal System Ref K120074
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Skeletal Design Partnership, Ltd. have in the registry?
The registry currently lists 1 device for The Skeletal Design Partnership, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Skeletal Design Partnership, Ltd.'s devices?
Among its 1 most recently registered device, The Skeletal Design Partnership, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do The Skeletal Design Partnership, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Skeletal Design Partnership, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Skeletal Design Partnership, Ltd. in the registry?
The most recently registered devices listed for The Skeletal Design Partnership, Ltd. include FOUNDATION SPINAL SYSTEM.