A Johnson & Johnson Company
Country not established
- Devices
- 1
What A Johnson & Johnson Company makes
The company manufactures the SKYLINE Anterior Cervical Plate System, a Class II orthopedic device designed for internal spinal fixation in cervical spine surgeries.
This device is regulated under the FDA’s 510(k) pathway as a Class II medical device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Skyline Anterior Cervical Plate System Ref K103491
510(k) 510(k)
Frequently asked questions
How many devices does A Johnson & Johnson Company have in the registry?
The registry currently lists 1 device for A Johnson & Johnson Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list A Johnson & Johnson Company's devices?
Among its 1 most recently registered device, A Johnson & Johnson Company has devices listed in FDA 510(k) (1 device).
What risk classes do A Johnson & Johnson Company's devices fall under?
Among its 1 most recently registered device, the classes recorded for A Johnson & Johnson Company's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A Johnson & Johnson Company in the registry?
The most recently registered devices listed for A Johnson & Johnson Company include SKYLINE ANTERIOR CERVICAL PLATE SYSTEM.