Anatomica AB
Country not established
- Devices
- 1
What Anatomica AB makes
Anatomica AB manufactures the Anatomica Posterior Cervical Fixation System, a device designed for spinal stabilization in the cervical region, providing surgical support for spinal fusion procedures.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. Anatomica AB is based in the United States.
Catalogue
Anatomica Posterior Cervical Fixation System Ref K061943
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anatomica AB have in the registry?
The registry currently lists 1 device for Anatomica AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anatomica AB's devices?
Among its 1 most recently registered device, Anatomica AB has devices listed in FDA 510(k) (1 device).
What risk classes do Anatomica AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Anatomica AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anatomica AB in the registry?
The most recently registered devices listed for Anatomica AB include ANATOMICA POSTERIOR CERVICAL FIXATION SYSTEM.