Medtronic Vertelink, Inc.
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- Devices
- 1
What Medtronic Vertelink, Inc. makes
Medtronic Vertelink, Inc. manufactures the KOBRA GPS Fixation System, a spinal fixation device designed for surgical stabilization of the spine.
The KOBRA GPS Fixation System is classified as a Class II medical device and is listed under FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Kobra Gps Fixation System Ref K042859
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Vertelink, Inc. have in the registry?
The registry currently lists 1 device for Medtronic Vertelink, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Vertelink, Inc.'s devices?
Among its 1 most recently registered device, Medtronic Vertelink, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Vertelink, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Vertelink, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Vertelink, Inc. in the registry?
The most recently registered devices listed for Medtronic Vertelink, Inc. include KOBRA GPS FIXATION SYSTEM.