Nutech Spine and Biologics
Country not established
- Devices
- 1
What Nutech Spine and Biologics makes
Nutech Spine and Biologics manufactures internal fixation devices, including the Anterior Cervical Plate System, designed for spinal stabilization in cervical spine surgeries. These products are intended for use in surgical procedures to support bone alignment and promote fusion in the neck region.
The company’s portfolio is regulated under Class II medical devices in the United States, with relevant products listed via the FDA’s 510(k) clearance pathway. The manufacturer operates from the US, adhering to regulatory requirements for spinal fixation hardware.
Catalogue
Anterior Cervical Plate System Ref K202972
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nutech Spine and Biologics have in the registry?
The registry currently lists 1 device for Nutech Spine and Biologics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nutech Spine and Biologics's devices?
Among its 1 most recently registered device, Nutech Spine and Biologics has devices listed in FDA 510(k) (1 device).
What risk classes do Nutech Spine and Biologics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nutech Spine and Biologics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nutech Spine and Biologics in the registry?
The most recently registered devices listed for Nutech Spine and Biologics include Anterior Cervical Plate System.