Medical Device Manufacturer · US , Superior , CO

Practical Navigation, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
1
Total
1
Cleared
0
Denied

Practical Navigation, LLC has 1 FDA 510(k) cleared medical devices. Based in Superior, US.

Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Practical Navigation, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Phiama, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Practical Navigation, LLC

1 devices
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