Pantheon Spinal is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pantheon Spinal - FDA 510(k) Cleared Devices
Recent clearances: Pantheon Pedicle Screw and Iliac Bolt Fixation System, Pantheon IBFD, Pantheon Spinal Pontus Interbody Fusion Device
4
Total
4
Cleared
0
Denied
Pantheon Spinal has 4 FDA 510(k) cleared medical devices. Based in Austin, US.
Latest FDA clearance: Jul 2024. Active since 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pantheon Spinal Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Djj Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pantheon Spinal
4 devices