Nervomatrix, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Nervomatrix, Ltd. makes
Nervomatrix, Ltd. manufactures the NEMA-ST (Model V1.0.2), a device designed for spinal alignment and surgical planning in orthopedic procedures.
The NEMA-ST device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Nema-St, Model V1.0.2 Ref K100668
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nervomatrix, Ltd. have in the registry?
The registry currently lists 1 device for Nervomatrix, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nervomatrix, Ltd.'s devices?
Among its 1 most recently registered device, Nervomatrix, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Nervomatrix, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nervomatrix, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nervomatrix, Ltd. in the registry?
The most recently registered devices listed for Nervomatrix, Ltd. include NEMA-ST, MODEL V1.0.2.