Kahtnu Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kahtnu Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CHENA-C Spacer System, KASILOF Cervical Plate System
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.
FDA 510(k) Regulatory Record - Kahtnu Surgical, Inc.
2 devices