Orothmet, Inc.
Country not established
- Devices
- 1
What Orothmet, Inc. makes
Orothmet, Inc. manufactures the MODIFICATION AXIOM TOTAL KNEE SYSTEM with a patellar component, a knee replacement device designed for total knee arthroplasty procedures.
This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orothmet, Inc. have in the registry?
The registry currently lists 1 device for Orothmet, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orothmet, Inc.'s devices?
Among its 1 most recently registered device, Orothmet, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orothmet, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orothmet, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orothmet, Inc. in the registry?
The most recently registered devices listed for Orothmet, Inc. include MODIFICATION AXIOM TOTAL KNEE SYST, PATELLAR COMP.