Nlt Spine, Ltd.
Country not established
- Devices
- 8
What Nlt Spine, Ltd. makes
Nlt Spine, Ltd. manufactures spinal fusion devices and systems, specifically the Prow Fusion-L, Prow Fusion, Prow Fusion-V, and the Espin system.
These products are classified as Class II medical devices and are listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Prow Fusion-L Ref K153665
Regimes: 510(k) Registry: 510(k)Prow Fusion Ref K151654
Regimes: 510(k) Registry: 510(k)Prow Fusion-V Ref K153786
Regimes: 510(k) Registry: 510(k)Espin Ref K130057
Regimes: 510(k) Registry: 510(k)Espin System Ref K133061
Regimes: 510(k) Registry: 510(k)Prow Fusion Ref K112359
Regimes: 510(k) Registry: 510(k)Prow Fusion Ref K130254
Regimes: 510(k) Registry: 510(k)Espin Ref K120553
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nlt Spine, Ltd. have in the registry?
The registry currently lists 8 devices for Nlt Spine, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nlt Spine, Ltd.'s devices?
Among its 8 most recently registered devices, Nlt Spine, Ltd. has devices listed in FDA 510(k) (8 devices).
What risk classes do Nlt Spine, Ltd.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Nlt Spine, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nlt Spine, Ltd. in the registry?
The most recently registered devices listed for Nlt Spine, Ltd. include PROW FUSION-L, PROW FUSION, PROW FUSION-V and ESPIN.