Monogram Orthopaedics, Inc.
Country not established
- Devices
- 1
What Monogram Orthopaedics, Inc. makes
Monogram Orthopaedics, Inc. makes the mBôs TKA System, a total knee arthroplasty device designed for knee replacement surgery.
The mBôs TKA System is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
mBôs (Monogram mBôs TKA System) Ref K242121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Monogram Orthopaedics, Inc. have in the registry?
The registry currently lists 1 device for Monogram Orthopaedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Monogram Orthopaedics, Inc.'s devices?
Among its 1 most recently registered device, Monogram Orthopaedics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Monogram Orthopaedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Monogram Orthopaedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Monogram Orthopaedics, Inc. in the registry?
The most recently registered devices listed for Monogram Orthopaedics, Inc. include mBôs (Monogram mBôs TKA System).