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Pantheon Spinal

FDA Regulatory Profile

Pantheon Spinal appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 26, 2024.

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

FDA data resources