Spinal Balance, Inc. is one of 18445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spinal Balance, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Libra Pedicle Screw System, Libra Pedicle Screw System
2
Total
2
Cleared
0
Denied
Spinal Balance, Inc. has 2 FDA 510(k) cleared medical devices. Based in Toledo, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinal Balance, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Spinal Balance, Inc.
2 devices