Spinal Stability, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spinal Stability, LLC - FDA 510(k) Cleared Devices
Recent clearances: MODULIF-A Anterior Lumbar Interbody Fusion System
1
Total
1
Cleared
0
Denied
Spinal Stability, LLC has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinal Stability, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Spinal Stability, LLC
1 devices