Montross Extremity Medical
Country not established
- Devices
- 1
What Montross Extremity Medical makes
Montross Extremity Medical manufactures the Hemi Implant System, which is a medical device designed for extremity applications.
The company is based in the United States, and its portfolio includes Class II devices that are listed in the FDA 510(k) regulatory registry.
Catalogue
Montross Extremity Medical Hemi Implant System Ref K221220
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Montross Extremity Medical have in the registry?
The registry currently lists 1 device for Montross Extremity Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Montross Extremity Medical's devices?
Among its 1 most recently registered device, Montross Extremity Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Montross Extremity Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Montross Extremity Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Montross Extremity Medical in the registry?
The most recently registered devices listed for Montross Extremity Medical include Montross Extremity Medical Hemi Implant System.