Sagico VA USA, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Sagico VA USA, LLC makes
Sagico VA USA, LLC manufactures spinal fixation devices, including the Titus Titanium Cervical, SAGICO Spinal System, and Ripley Spinal Screw System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Titus Titanium Cervical by SAGICO Ref K221138
Regimes: 510(k) Registry: 510(k)SAGICO Spinal System Ref K223143
Regimes: 510(k) Registry: 510(k)Ripley Spinal Screw System by SAGICO Ref K232561
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sagico VA USA, LLC have in the registry?
The registry currently lists 3 devices for Sagico VA USA, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sagico VA USA, LLC's devices?
Among its 3 most recently registered devices, Sagico VA USA, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Sagico VA USA, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sagico VA USA, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sagico VA USA, LLC in the registry?
The most recently registered devices listed for Sagico VA USA, LLC include Titus Titanium Cervical by SAGICO, SAGICO Spinal System and Ripley Spinal Screw System by SAGICO.