Legend Spine Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Legend Spine Technologies - FDA 510(k) Cleared Devices
Recent clearances: CORNICE Cervical Spacer System, STYLO Interbody Fusion Device
2
Total
2
Cleared
0
Denied
Legend Spine Technologies has 2 FDA 510(k) cleared medical devices. Based in Bethlehem, US.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Legend Spine Technologies Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mrc/X, LLC and Mrc-X, LLC.
FDA 510(k) Regulatory Record - Legend Spine Technologies
2 devices