Medtronic Midas Rex
Country not established
- Devices
- 1
What Medtronic Midas Rex makes
Medtronic Midas Rex produces orthopedic surgical systems, including pneumatic high-speed drills and related instrumentation designed for bone preparation and joint surgery.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Medtronic Mida Rex Legend System, Midas Rex Legend Pneumatic High Speed System Or Legend System Ref K020069
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Midas Rex have in the registry?
The registry currently lists 1 device for Medtronic Midas Rex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Midas Rex's devices?
Among its 1 most recently registered device, Medtronic Midas Rex has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Midas Rex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Midas Rex's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Midas Rex in the registry?
The most recently registered devices listed for Medtronic Midas Rex include MEDTRONIC MIDA REX LEGEND SYSTEM, MIDAS REX LEGEND PNEUMATIC HIGH SPEED SYSTEM OR LEGEND SYSTEM.