Verticor, Ltd.
Country not established
- Devices
- 3
What Verticor, Ltd. makes
Verticor, Ltd. manufactures spinal fixation devices, including the Cervicore Corpectomy Cage for cervical spine reconstruction, the Verticor K-Wire System for surgical stabilization, and the Venus Anterior Cervical Plate for anterior cervical support.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cervicore Corpectomy Cage Ref K091426
Regimes: 510(k) Registry: 510(k)Verticor K-Wire System Ref K110047
Regimes: 510(k) Registry: 510(k)Venus Anterior Cervical Plate Ref K103137
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verticor, Ltd. have in the registry?
The registry currently lists 3 devices for Verticor, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verticor, Ltd.'s devices?
Among its 3 most recently registered devices, Verticor, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Verticor, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Verticor, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verticor, Ltd. in the registry?
The most recently registered devices listed for Verticor, Ltd. include CERVICORE CORPECTOMY CAGE, VERTICOR K-WIRE SYSTEM and VENUS ANTERIOR CERVICAL PLATE.