Laura Cattabriga is one of 20333 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laura Cattabriga - FDA 510(k) Cleared Devices
Recent clearances: CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM, BONE FRAGMENT AND FIXATION PLATES, SCREWS AND WASHERS
2
Total
2
Cleared
0
Denied
Laura Cattabriga has 2 FDA 510(k) cleared medical devices. Based in N. Bay Village, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Laura Cattabriga Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laura Cattabriga
2 devices