Footbridge Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Footbridge Medical - FDA 510(k) Cleared Devices
Recent clearances: HyperFlex™ Bunion Correction System
1
Total
1
Cleared
0
Denied
Footbridge Medical has 1 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Footbridge Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Footbridge Medical
1 devices