Laura Cattabriga
Country not established
- Devices
- 2
What Laura Cattabriga makes
Laura Cattabriga manufactures orthopedic fixation systems, including cannulated screws and Kirschner (K-wire) systems for bone stabilization, as well as bone fragment fixation plates, screws, and washers for fracture management.
These devices are classified as Class II under FDA regulations and are recorded in the 510(k) premarket notification database. The manufacturer operates from the United States.
Catalogue
Cannulated Screw And Kirschner (Kwire) System Ref K130613
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laura Cattabriga have in the registry?
The registry currently lists 2 devices for Laura Cattabriga. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laura Cattabriga's devices?
Among its 2 most recently registered devices, Laura Cattabriga has devices listed in FDA 510(k) (2 devices).
What risk classes do Laura Cattabriga's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Laura Cattabriga's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laura Cattabriga in the registry?
The most recently registered devices listed for Laura Cattabriga include CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM and BONE FRAGMENT AND FIXATION PLATES, SCREWS AND WASHERS.