Mircoport Orthopedics, Inc.
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- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
EVOLUTION NitrX Medial-Pivot Knee Ref K182251
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mircoport Orthopedics, Inc. have in the registry?
The registry currently lists 1 device for Mircoport Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mircoport Orthopedics, Inc.'s devices?
Among its 1 most recently registered device, Mircoport Orthopedics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mircoport Orthopedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mircoport Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mircoport Orthopedics, Inc. in the registry?
The most recently registered devices listed for Mircoport Orthopedics, Inc. include EVOLUTION NitrX Medial-Pivot Knee.