Arrowhead De, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrowhead De, LLC - FDA 510(k) Cleared Devices
Recent clearances: Accessories for the SixFix® Hexapod Fixator, SixFix™ Hexapod Fixator and Deformity Analysis and Correction Software (DACS)
3
Total
3
Cleared
0
Denied
Arrowhead De, LLC has 3 FDA 510(k) cleared medical devices. Based in Collierville, US.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Arrowhead De, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrowhead De, LLC
3 devices