Back 2 Basics Direct, LLC is one of 12989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Back 2 Basics Direct, LLC - FDA 510(k) Cleared Devices
Recent clearances: Dymaxeon Spine System, eCarbon IBDs, Dymaxeon Spine System
4
Total
4
Cleared
0
Denied
Back 2 Basics Direct, LLC has 4 FDA 510(k) cleared medical devices. Based in Independence, US.
Historical record: 4 cleared submissions from 2015 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Back 2 Basics Direct, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Backroads Consulting, Musculoskeletal Clinical Regulatory Advisers, LLC and Jalex Medical.
FDA 510(k) Regulatory Record - Back 2 Basics Direct, LLC
4 devices