Medical Device Manufacturer · US , Colorado Springs , CO

Montross Extremity Medical - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
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
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