Alfred O. Bonati, M.D.
Country not established
- Devices
- 1
What Alfred O. Bonati, M.D. makes
The company develops and provides arthroscopic lumbar discectomy devices, including mechanical and laser-assisted systems designed for spinal surgery. These tools are used to remove herniated or damaged disc material while preserving surrounding spinal structures.
The portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Alfred O. Bonati, M.D. have in the registry?
The registry currently lists 1 device for Alfred O. Bonati, M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alfred O. Bonati, M.D.'s devices?
Among its 1 most recently registered device, Alfred O. Bonati, M.D. has devices listed in FDA 510(k) (1 device).
What risk classes do Alfred O. Bonati, M.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alfred O. Bonati, M.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alfred O. Bonati, M.D. in the registry?
The most recently registered devices listed for Alfred O. Bonati, M.D. include ARTHROSCOPIC LUMBAR MECHANICAL AND LASER DISCECTOM.