Nutech Spine and Biologics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nutech Spine and Biologics - FDA 510(k) Cleared Devices
Recent clearances: Anterior Cervical Plate System
1
Total
1
Cleared
0
Denied
Nutech Spine and Biologics has 1 FDA 510(k) cleared medical devices. Based in Birmingham, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Nutech Spine and Biologics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Surgop Support as regulatory consultant.
FDA 510(k) Regulatory Record - Nutech Spine and Biologics
1 devices