Interbody Innovations, LLP
United StatesFDA applicant, unverified
- Devices
- 4
What Interbody Innovations, LLP makes
Interbody Innovations, Llp manufactures spinal fusion devices including ZEUS small cervical cage and various lumbar cages (large, extra-large, curved, and straight), as well as spinal spheres and PEEK spinal spheres.
The company's products are classified as Class II and Class III medical devices and are listed in the FDA 510(k) registry. Interbody Innovations is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Spinal Spheres Ref K062992
Regimes: 510(k) Registry: 510(k)Peek Spinal Spheres Ref K073105
Regimes: 510(k) Registry: 510(k)Interbody Innovations Cement Restrictor Ref K051371
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Interbody Innovations, Llp have in the registry?
The registry currently lists 4 devices for Interbody Innovations, Llp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interbody Innovations, Llp's devices?
Among its 4 most recently registered devices, Interbody Innovations, Llp has devices listed in FDA 510(k) (4 devices).
What risk classes do Interbody Innovations, Llp's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Interbody Innovations, Llp's devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Interbody Innovations, Llp in the registry?
The most recently registered devices listed for Interbody Innovations, Llp include ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGES, SPINAL SPHERES, PEEK SPINAL SPHERES and INTERBODY INNOVATIONS CEMENT RESTRICTOR.