Medtronic Surgical Navigation
Country not established
- Devices
- 3
What Medtronic Surgical Navigation makes
Medtronic Surgical Navigation manufactures the StealthStation treatment guidance platform, including modifications to the platform and the StealthStation wireless surgeon mouse.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Stelthstation Wireless Surgeon Mouse Ref K051029
Regimes: 510(k) Registry: 510(k)Steathstation Treatment Guidance Platform Ref K001801
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Surgical Navigation have in the registry?
The registry currently lists 3 devices for Medtronic Surgical Navigation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Surgical Navigation's devices?
Among its 3 most recently registered devices, Medtronic Surgical Navigation has devices listed in FDA 510(k) (3 devices).
What risk classes do Medtronic Surgical Navigation's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medtronic Surgical Navigation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Surgical Navigation in the registry?
The most recently registered devices listed for Medtronic Surgical Navigation include MODIFICATION TO STEATHSTATION TREATMENT GUIDANCE PLATFORM, STELTHSTATION WIRELESS SURGEON MOUSE and STEATHSTATION TREATMENT GUIDANCE PLATFORM.