Lntelivation, LLC
Country not established
- Devices
- 1
What Lntelivation, LLC makes
Lntelivation, LLC makes the Advantage-C PEEK Cervical Interbody Fusion Device, which is a spinal implant used for cervical interbody fusion procedures.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lntelivation, LLC have in the registry?
The registry currently lists 1 device for Lntelivation, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lntelivation, LLC's devices?
Among its 1 most recently registered device, Lntelivation, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Lntelivation, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lntelivation, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lntelivation, LLC in the registry?
The most recently registered devices listed for Lntelivation, LLC include Advantage-C PEEK Cervical lnterbody Fusion Device.