Johnson
Country not established
- Devices
- 1
What Johnson makes
Johnson manufactures the BLOCK™ Arthroscopic Tool Kit, a specialized set of instruments designed for arthroscopic surgical procedures. These tools are intended for use in joint surgeries, such as those involving the knee, shoulder, or other articulations, to facilitate minimally invasive techniques.
The BLOCK™ Arthroscopic Tool Kit is classified as a Class II medical device under FDA regulations and has been submitted for clearance via the 510(k) pathway. The company is based in the United States.
Catalogue
Block(Tm) Arthroscopic Tool Kit Ref K946174
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Johnson have in the registry?
The registry currently lists 1 device for Johnson. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johnson's devices?
Among its 1 most recently registered device, Johnson has devices listed in FDA 510(k) (1 device).
What risk classes do Johnson's devices fall under?
Among its 1 most recently registered device, the classes recorded for Johnson's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Johnson in the registry?
The most recently registered devices listed for Johnson include BLOCK(TM) ARTHROSCOPIC TOOL KIT.