Omni Surgical, LLC Dba Spine360
United StatesFDA applicant, unverified
- Devices
- 2
What Omni Surgical, LLC Dba Spine360 makes
Omni Surgical, LLC (dba Spine360) manufactures the KESTREL Posterior Cervical Spine System, a device designed for surgical applications in the cervical spine region, intended to provide stabilization and support.
The KESTREL Posterior Cervical Spine System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Stingray Cervical Cage Ref K122085
Regimes: 510(k) Registry: 510(k)Kestrel Posterior Cervical Spine System Ref K132122
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omni Surgical, LLC Dba Spine360 have in the registry?
The registry currently lists 2 devices for Omni Surgical, LLC Dba Spine360. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni Surgical, LLC Dba Spine360's devices?
Among its 2 most recently registered devices, Omni Surgical, LLC Dba Spine360 has devices listed in FDA 510(k) (2 devices).
What risk classes do Omni Surgical, LLC Dba Spine360's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Omni Surgical, LLC Dba Spine360's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omni Surgical, LLC Dba Spine360 in the registry?
The most recently registered devices listed for Omni Surgical, LLC Dba Spine360 include STINGRAY CERVICAL CAGE and KESTREL POSTERIOR CERVICAL SPINE SYSTEM.