Medtronic Inc., Neurological Division.
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- Devices
- 1
What Medtronic Inc., Neurological Division. makes
Medtronic Inc., Neurological Division manufactures compact test stimulation leads, specifically the Model 3873 1* 8 and Model 3874 1* 8.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Inc., Neurological Division. have in the registry?
The registry currently lists 1 device for Medtronic Inc., Neurological Division.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Inc., Neurological Division.'s devices?
Among its 1 most recently registered device, Medtronic Inc., Neurological Division. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Inc., Neurological Division.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Inc., Neurological Division.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Inc., Neurological Division. in the registry?
The most recently registered devices listed for Medtronic Inc., Neurological Division. include MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS.