Sync Surgical
Country not established
- Devices
- 1
What Sync Surgical makes
Sync Surgical develops the Cervical Interbody and Vertebral Body Replacement (VBR) Fusion System, a spinal implant designed for anterior cervical fusion and vertebral body replacement procedures.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Cervical Interbody and VBR Fusion System Ref K252219
510(k) 510(k)
Frequently asked questions
How many devices does Sync Surgical have in the registry?
The registry currently lists 1 device for Sync Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sync Surgical's devices?
Among its 1 most recently registered device, Sync Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Sync Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sync Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sync Surgical in the registry?
The most recently registered devices listed for Sync Surgical include Cervical Interbody and VBR Fusion System.