Orthocircle Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthocircle Spine - FDA 510(k) Cleared Devices
Recent clearances: OrthoCircle Spine Pedicle Screw System
1
Total
1
Cleared
0
Denied
Orthocircle Spine has 1 FDA 510(k) cleared medical devices. Based in Savannah, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthocircle Spine 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 - Orthocircle Spine
1 devices