Neurosurgical Devices, Inc.
Country not established
- Devices
- 1
What Neurosurgical Devices, Inc. makes
Neurosurgical Devices, Inc. makes the GOUDA FRAME FOR STEREOTACTIC NEUROSURGERY, a device used to stabilize and position the head during neurosurgical procedures.
The GOUDA FRAME FOR STEREOTACTIC NEUROSURGERY is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Gouda Frame For Stereotactic Neurosurgery Ref K852662
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurosurgical Devices, Inc. have in the registry?
The registry currently lists 1 device for Neurosurgical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurosurgical Devices, Inc.'s devices?
Among its 1 most recently registered device, Neurosurgical Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neurosurgical Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurosurgical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurosurgical Devices, Inc. in the registry?
The most recently registered devices listed for Neurosurgical Devices, Inc. include GOUDA FRAME FOR STEREOTACTIC NEUROSURGERY.