Spinal USA, LLC
United StatesFDA applicant, unverified
- Devices
- 24
What Spinal USA, LLC makes
Spinal USA, LLC manufactures the Slimplicity Solo Anterior Cervical Plate System, which is a spinal fixation device.
This device is classified as a Class II medical device and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Search and filter all 24 devicesFrequently asked questions
How many devices does Spinal USA, LLC have in the registry?
The registry currently lists 24 devices for Spinal USA, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinal USA, LLC's devices?
Among its 24 most recently registered devices, Spinal USA, LLC has devices listed in FDA 510(k) (24 devices).
What risk classes do Spinal USA, LLC's devices fall under?
Among its 24 most recently registered devices, the classes recorded for Spinal USA, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinal USA, LLC in the registry?
The most recently registered devices listed for Spinal USA, LLC include SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE, SPINAL USA INTERBODY FUSION DEVICE, MODIFICATION TO: PSS SYSTEM and VAULT ALIF SYSTEM.