Signus Medical
Country not established
- Devices
- 8
What Signus Medical makes
Signus Medical manufactures spinal fixation devices, including the DIANA FUSION CAGE—a spinal interbody fusion cage—and the MONOPOLY PEDICLE SCREW SYSTEM, designed for internal fixation in spinal surgeries.
These products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Monopoly Pedicle Screw System Ref K081108
Regimes: 510(k) Registry: 510(k)Tetris Spinal Implant Ref K022793
Regimes: 510(k) Registry: 510(k)Peek Tetris Spinal Implant Ref K031757
Regimes: 510(k) Registry: 510(k)Rabea Cement Restrictor Ref K020836
Regimes: 510(k) Registry: 510(k)Nubic Spinal Implant Ref K052096
Regimes: 510(k) Registry: 510(k)Conklusion Pedicle Screw System Ref K031455
Regimes: 510(k) Registry: 510(k)Diana Fusion Cage Ref K091122
Regimes: 510(k) Registry: 510(k)Monopoly Pedicle Screw System Ref K092073
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Signus Medical have in the registry?
The registry currently lists 8 devices for Signus Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Signus Medical's devices?
Among its 8 most recently registered devices, Signus Medical has devices listed in FDA 510(k) (8 devices).
What risk classes do Signus Medical's devices fall under?
Among its 8 most recently registered devices, the classes recorded for Signus Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Signus Medical in the registry?
The most recently registered devices listed for Signus Medical include MONOPOLY PEDICLE SCREW SYSTEM, TETRIS SPINAL IMPLANT, PEEK TETRIS SPINAL IMPLANT and RABEA CEMENT RESTRICTOR.