Orthobond Coporation
Country not established
- Devices
- 1
What Orthobond Coporation makes
Orthobond Corporation manufactures the Orthobond Mariner Pedicle Screw System, a spinal fixation device used for orthopedic surgical applications in the lumbar and thoracic spine.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Orthobond Mariner Pedicle Screw System Ref DEN220015
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Orthobond Coporation have in the registry?
The registry currently lists 1 device for Orthobond Coporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthobond Coporation's devices?
Among its 1 most recently registered device, Orthobond Coporation has devices listed in FDA 510(k) (1 device).
What risk classes do Orthobond Coporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthobond Coporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthobond Coporation in the registry?
The most recently registered devices listed for Orthobond Coporation include Orthobond Mariner Pedicle Screw System.