Osteonics Reconstructive Products Div.
Country not established
- Devices
- 2
What Osteonics Reconstructive Products Div. makes
The company manufactures orthopedic reconstruction devices, including glenoid components for shoulder arthroplasty and proximal cement spacers for joint replacement procedures.
These products are classified as Class II medical devices and are listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Osteonics Sr Glenoid Components Ref K903886
Regimes: 510(k) Registry: 510(k)Proximal Cement Spacer Ref K895378
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteonics Reconstructive Products Div. have in the registry?
The registry currently lists 2 devices for Osteonics Reconstructive Products Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteonics Reconstructive Products Div.'s devices?
Among its 2 most recently registered devices, Osteonics Reconstructive Products Div. has devices listed in FDA 510(k) (2 devices).
What risk classes do Osteonics Reconstructive Products Div.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Osteonics Reconstructive Products Div.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteonics Reconstructive Products Div. in the registry?
The most recently registered devices listed for Osteonics Reconstructive Products Div. include OSTEONICS SR GLENOID COMPONENTS and PROXIMAL CEMENT SPACER.