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Bright Spine

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221542Galileo Vertebral Body Replacement DeviceJanuary 13, 2023
K192145Galileo Vertebral Body Replacement DeviceApril 21, 2020
K102449BRIGHT SPINE GALILEO SPINAL SPACER SYSTEMFebruary 11, 2011