Kahtnu Surgical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Kahtnu Surgical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Soldotna, US.
Last cleared in 2021. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kahtnu Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.
2 devices