North American Medical Corp (Nam)
United StatesFDA applicant, unverified
- Devices
- 3
What North American Medical Corp (Nam) makes
North American Medical Corp (Nam) makes the Model D Disc Force and the Spina System.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Spina System Ref K002260
Regimes: 510(k) Registry: 510(k)Model D Disc Force Ref K073132
Regimes: 510(k) Registry: 510(k)Spina System Ref K033231
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does North American Medical Corp (Nam) have in the registry?
The registry currently lists 3 devices for North American Medical Corp (Nam). Devices recorded under merged duplicate company entries are counted once.
Which registries list North American Medical Corp (Nam)'s devices?
Among its 3 most recently registered devices, North American Medical Corp (Nam) has devices listed in FDA 510(k) (3 devices).
What risk classes do North American Medical Corp (Nam)'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for North American Medical Corp (Nam)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from North American Medical Corp (Nam) in the registry?
The most recently registered devices listed for North American Medical Corp (Nam) include SPINA SYSTEM and MODEL D DISC FORCE.