Medtronic A/S
DenmarkFDA applicant, unverified
- Devices
- 1
What Medtronic A/S makes
Medtronic A/S makes the CLAVIS device, which is a medical device product.
The CLAVIS device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Clavis Ref K062478
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic A/S have in the registry?
The registry currently lists 1 device for Medtronic A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic A/S's devices?
Among its 1 most recently registered device, Medtronic A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic A/S in the registry?
The most recently registered devices listed for Medtronic A/S include CLAVIS.