Medtronic Surgical Technologies
Country not established
- Devices
- 1
What Medtronic Surgical Technologies makes
Medtronic Surgical Technologies manufactures the TRITON Electric High Torque Handpiece, a powered surgical instrument designed for precision cutting and drilling in orthopedic and spinal procedures. The device integrates with compatible software modules to enhance surgical workflows, supporting tasks such as bone preparation and implant placement.
The TRITON Electric High Torque Handpiece is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Surgical Technologies have in the registry?
The registry currently lists 1 device for Medtronic Surgical Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Surgical Technologies's devices?
Among its 1 most recently registered device, Medtronic Surgical Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Surgical Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Surgical Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Surgical Technologies in the registry?
The most recently registered devices listed for Medtronic Surgical Technologies include TRITON ELECTRIC HIGH TORQUE HANDPIECE AND SOFTWARE MODULE.