Montross Extremity Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Montross Extremity Medical - FDA 510(k) Cleared Devices
Recent clearances: Montross Extremity Medical Hemi Implant System
1
Total
1
Cleared
0
Denied
Montross Extremity Medical has 1 FDA 510(k) cleared medical devices. Based in Colorado Springs, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Montross Extremity Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intrepid Orthopedics, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Montross Extremity Medical
1 devices