Ascent Medical, LLC is one of 20186 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ascent Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: PHIN-FX Cannulated Lag Screw System
1
Total
1
Cleared
0
Denied
Ascent Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Jackson, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ascent Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Engineering Consulting Services, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ascent Medical, LLC
1 devices