Austin Miller Trauma, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Austin Miller Trauma, LLC - FDA 510(k) Cleared Devices
Recent clearances: Austin Miller Large External Fixation System
1
Total
1
Cleared
0
Denied
Austin Miller Trauma, LLC has 1 FDA 510(k) cleared medical devices. Based in Germantown, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Austin Miller Trauma, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Austin Miller Trauma, LLC
1 devices