Arthro Kinetics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Arthro Kinetics, Inc. makes
Arthro Kinetics, Inc. makes the Arthro Kinetics Vesalius MR Generator and its accessories, as well as an endoscopic spine system.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Endoscopic Spine System Ref K061246
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthro Kinetics, Inc. have in the registry?
The registry currently lists 2 devices for Arthro Kinetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthro Kinetics, Inc.'s devices?
Among its 2 most recently registered devices, Arthro Kinetics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arthro Kinetics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arthro Kinetics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthro Kinetics, Inc. in the registry?
The most recently registered devices listed for Arthro Kinetics, Inc. include ARTHRO KINETICS VESALIUS MR GENERATOR, MODELS 2004-2006; ACCESSORIES FOR MR GENERATOR and ENDOSCOPIC SPINE SYSTEM.