Retrofix Screws, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Retrofix Screws, LLC - FDA 510(k) Cleared Devices
Recent clearances: RetroFix
1
Total
1
Cleared
0
Denied
Retrofix Screws, LLC has 1 FDA 510(k) cleared medical devices. Based in Salisbury, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Retrofix Screws, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Fish & Richardson, P.C. as regulatory consultant.
FDA 510(k) Regulatory Record - Retrofix Screws, LLC
1 devices