Kenneth J. Hoek, M.D., Inc.
Country not established
- Devices
- 1
What Kenneth J. Hoek, M.D., Inc. makes
The company manufactures specialized femoral cement removal instruments, designed for orthopedic surgical procedures to remove bone cement from the femur during revisions or corrections.
These instruments are classified as Class I devices under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Femoral Cement Removal Instruments Ref K870217
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kenneth J. Hoek, M.D., Inc. have in the registry?
The registry currently lists 1 device for Kenneth J. Hoek, M.D., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kenneth J. Hoek, M.D., Inc.'s devices?
Among its 1 most recently registered device, Kenneth J. Hoek, M.D., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kenneth J. Hoek, M.D., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kenneth J. Hoek, M.D., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kenneth J. Hoek, M.D., Inc. in the registry?
The most recently registered devices listed for Kenneth J. Hoek, M.D., Inc. include FEMORAL CEMENT REMOVAL INSTRUMENTS.