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Pantheon Spinal

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241494Pantheon Pedicle Screw and Iliac Bolt Fixation SystemJuly 26, 2024
K203003Pantheon IBFDJuly 7, 2021
K181548Pantheon Spinal Pontus Interbody Fusion DeviceDecember 16, 2019
K113781PANTHEON SPINAL IBFD SYSTEMApril 26, 2013