Xerxes Arthopedix, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xerxes Arthopedix, LLC - FDA 510(k) Cleared Devices
Recent clearances: Xerxes Hip Stem
1
Total
1
Cleared
0
Denied
Xerxes Arthopedix, LLC has 1 FDA 510(k) cleared medical devices. Based in Naples, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Xerxes Arthopedix, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xerxes Arthopedix, LLC
1 devices