Practical Navigation, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Practical Navigation, LLC - FDA 510(k) Cleared Devices
Recent clearances: Practical Navigation Surgical Guidance System (PNSGS)
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