Northo Orthopedics
Country not established
- Devices
- 1
What Northo Orthopedics makes
Northo Orthopedics manufactures orthopedic bone screws designed for internal fixation in fracture stabilization and joint reconstruction procedures. These devices are intended for use in surgical applications requiring secure bone attachment, such as long bone fractures or arthroplasty.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Northo Bone Screw Ref K925872
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Northo Orthopedics have in the registry?
The registry currently lists 1 device for Northo Orthopedics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Northo Orthopedics's devices?
Among its 1 most recently registered device, Northo Orthopedics has devices listed in FDA 510(k) (1 device).
What risk classes do Northo Orthopedics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Northo Orthopedics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Northo Orthopedics in the registry?
The most recently registered devices listed for Northo Orthopedics include NORTHO BONE SCREW.