Fix Surgical
Country not established
- Devices
- 2
What Fix Surgical makes
Fix Surgical manufactures the Augment Off-Axis Instrument System, a surgical tool designed for precise off-axis visualization and manipulation in minimally invasive procedures.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is registered in the United States.
Catalogue
Augment Off-Axis Instrument System Ref K233148
Regimes: 510(k) Registry: 510(k)Augment Off-Axis Instrument System Ref K241043
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fix Surgical have in the registry?
The registry currently lists 2 devices for Fix Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fix Surgical's devices?
Among its 2 most recently registered devices, Fix Surgical has devices listed in FDA 510(k) (2 devices).
What risk classes do Fix Surgical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fix Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fix Surgical in the registry?
The most recently registered devices listed for Fix Surgical include Augment Off-Axis Instrument System.