Sanacor
Country not established
- Devices
- 3
What Sanacor makes
Sanacor manufactures orthopedic fixation systems for spinal surgery, including pedicle screw systems and anterior cervical plating solutions designed for spinal stabilization procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Alpine Pedicle Screw System Ref K090477
Regimes: 510(k) Registry: 510(k)Active Anterior Cervical Plate System Ref K073500
Regimes: 510(k) Registry: 510(k)Lowtop Pedicle Screw System Ref K070933
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanacor have in the registry?
The registry currently lists 3 devices for Sanacor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanacor's devices?
Among its 3 most recently registered devices, Sanacor has devices listed in FDA 510(k) (3 devices).
What risk classes do Sanacor's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sanacor's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanacor in the registry?
The most recently registered devices listed for Sanacor include ALPINE PEDICLE SCREW SYSTEM, ACTIVE ANTERIOR CERVICAL PLATE SYSTEM and LOWTOP PEDICLE SCREW SYSTEM.