Core-Nexus
Country not established
- Devices
- 2
What Core-Nexus makes
Core-Nexus manufactures orthopedic fixation systems, including the NEXUS Anterior Cervical Plate System for spinal stabilization and the CORE Pedicle Screw System for vertebral fixation in spinal surgeries.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Nexus Anterior Cervical Plate System Ref K131520
Regimes: 510(k) Registry: 510(k)Core Pedicle Screw System Ref K131522
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Core-Nexus have in the registry?
The registry currently lists 2 devices for Core-Nexus. Devices recorded under merged duplicate company entries are counted once.
Which registries list Core-Nexus's devices?
Among its 2 most recently registered devices, Core-Nexus has devices listed in FDA 510(k) (2 devices).
What risk classes do Core-Nexus's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Core-Nexus's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Core-Nexus in the registry?
The most recently registered devices listed for Core-Nexus include NEXUS ANTERIOR CERVICAL PLATE SYSTEM and CORE PEDICLE SCREW SYSTEM.