John Riccio
Country not established
- Devices
- 3
What John Riccio makes
John Riccio manufactures orthopedic fixation devices, including the Fusion Medical Cannulated Screw System for bone stabilization and the Fusion Medical STI (Screw-Tightening Interface) for securing implants in spinal or long-bone procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Fusion Medical Cannulated Screw System Ref K081122
Regimes: 510(k) Registry: 510(k)Fusion Medical Ring Lock System Ref K100857
Regimes: 510(k) Registry: 510(k)Fusion Medical Sti Ref K081755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does John Riccio have in the registry?
The registry currently lists 3 devices for John Riccio. Devices recorded under merged duplicate company entries are counted once.
Which registries list John Riccio's devices?
Among its 3 most recently registered devices, John Riccio has devices listed in FDA 510(k) (3 devices).
What risk classes do John Riccio's devices fall under?
Among its 3 most recently registered devices, the classes recorded for John Riccio's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from John Riccio in the registry?
The most recently registered devices listed for John Riccio include FUSION MEDICAL CANNULATED SCREW SYSTEM, FUSION MEDICAL RING LOCK SYSTEM and FUSION MEDICAL STI.