Sij Surgical
Country not established
- Devices
- 1
What Sij Surgical makes
Sij Surgical manufactures the Outlet Sacroiliac Joint Fusion System, a device designed for sacroiliac joint fusion procedures to address chronic pain or instability.
The company’s portfolio is regulated under FDA Class II devices, with the Outlet Sacroiliac Joint Fusion System listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Outlet Sacroiliac Joint Fusion System Ref K181881
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sij Surgical have in the registry?
The registry currently lists 1 device for Sij Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sij Surgical's devices?
Among its 1 most recently registered device, Sij Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Sij Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sij Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sij Surgical in the registry?
The most recently registered devices listed for Sij Surgical include Outlet Sacroiliac Joint Fusion System.