Overture Orthopaedics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Overture Orthopaedics - FDA 510(k) Cleared Devices
Recent clearances: OvertureTi Knee Resurfacing SystemTM
1
Total
1
Cleared
0
Denied
Overture Orthopaedics has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Overture Orthopaedics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Overture Orthopaedics
1 devices