Spineway

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231658VEOS Spinal Fixation SystemOctober 10, 2023
K191726mont blanc & mont blanc MIS Spinal SystemsSeptember 12, 2019
K162694Ayers Rock Cervical interbody fusion systemJanuary 12, 2017
K161387Mont Blanc and Mont Blanc MIS Spinal SystemsAugust 4, 2016
K152355Twin Peaks Lumbar Interbody Fusion SystemDecember 10, 2015
K150185Mont Blanc Spinal SystemMay 12, 2015
K150036Blue Mountain Cervical Plate SystemMay 7, 2015