Senecka Spine is one of 20173 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Senecka Spine - FDA 510(k) Cleared Devices
Recent clearances: Seneka II Polyscrew Pedicle Fixation System, Seneka I Polyscrew Pedicle Fixation System
2
Total
2
Cleared
0
Denied
Senecka Spine has 2 FDA 510(k) cleared medical devices. Based in Johnson City, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Senecka Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Silver Pine Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Senecka Spine
2 devices