Presidio Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Presidio Surgical - FDA 510(k) Cleared Devices
Recent clearances: Viking Lumbar Polyaxial Screw System
1
Total
1
Cleared
0
Denied
Presidio Surgical has 1 FDA 510(k) cleared medical devices. Based in Alamo, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Presidio Surgical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Presidio Surgical
1 devices