N Spine, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What N Spine, Inc. makes
N Spine, Inc. makes spinal fixation systems, including the NGARDE System, NFIX Fusion System, and NFIX II Pedicle Screw System.
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
Ngarde System Ref K072685
510(k) 510(k)Nfix Fusion System Ref K053623
510(k) 510(k)Nfix Ii Pedicle Screw System Ref K061774
510(k) 510(k)
Frequently asked questions
How many devices does N Spine, Inc. have in the registry?
The registry currently lists 3 devices for N Spine, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list N Spine, Inc.'s devices?
Among its 3 most recently registered devices, N Spine, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do N Spine, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for N Spine, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from N Spine, Inc. in the registry?
The most recently registered devices listed for N Spine, Inc. include NGARDE SYSTEM, NFIX FUSION SYSTEM and NFIX II PEDICLE SCREW SYSTEM.