Jointpoint, Inc.
Country not established
- Devices
- 1
What Jointpoint, Inc. makes
Jointpoint, Inc. manufactures the JointPoint system, a medical device designed for intraoperative imaging and navigation during orthopedic procedures, particularly joint surgeries.
The device portfolio is classified as Class II under FDA regulations and is supported by 510(k) clearance. The company is based in the United States.
Catalogue
JointPoint Ref K160284
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jointpoint, Inc. have in the registry?
The registry currently lists 1 device for Jointpoint, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jointpoint, Inc.'s devices?
Among its 1 most recently registered device, Jointpoint, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jointpoint, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jointpoint, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jointpoint, Inc. in the registry?
The most recently registered devices listed for Jointpoint, Inc. include JointPoint.