Senecka Spine
Country not established
- Devices
- 2
What Senecka Spine makes
Senecka Spine manufactures pedicle fixation systems, including the Seneka II and Seneka I Polyscrew Pedicle Fixation Systems, designed for spinal stabilization procedures.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Seneka II Polyscrew Pedicle Fixation System Ref K153525
Regimes: 510(k) Registry: 510(k)Seneka I Polyscrew Pedicle Fixation System Ref K151849
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Senecka Spine have in the registry?
The registry currently lists 2 devices for Senecka Spine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Senecka Spine's devices?
Among its 2 most recently registered devices, Senecka Spine has devices listed in FDA 510(k) (2 devices).
What risk classes do Senecka Spine's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Senecka Spine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Senecka Spine in the registry?
The most recently registered devices listed for Senecka Spine include Seneka II Polyscrew Pedicle Fixation System and Seneka I Polyscrew Pedicle Fixation System.