Spine Next America Corporation
United StatesFDA applicant, unverified
- Devices
- 5
What Spine Next America Corporation makes
Spine Next America Corporation makes vertebral body replacement devices, including the FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5 and FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 1, 2, 3 AND 4.
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
Shiraz-Anterior System Ref K033965
Regimes: 510(k) Registry: 510(k)Shiraz-Java Spinal Fixation System Ref K033772
Regimes: 510(k) Registry: 510(k)Shiraz Posterior System Ref K033947
Regimes: 510(k) Registry: 510(k)Fidji-Vertebral Body Replacement Type 5 Ref K042713
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spine Next America Corporation have in the registry?
The registry currently lists 5 devices for Spine Next America Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spine Next America Corporation's devices?
Among its 5 most recently registered devices, Spine Next America Corporation has devices listed in FDA 510(k) (5 devices).
What risk classes do Spine Next America Corporation's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Spine Next America Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spine Next America Corporation in the registry?
The most recently registered devices listed for Spine Next America Corporation include SHIRAZ-ANTERIOR SYSTEM, SHIRAZ-JAVA SPINAL FIXATION SYSTEM, SHIRAZ POSTERIOR SYSTEM and FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5.