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Intrauma S.P.A

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K252959WRISTAR MultiAx Distal Radius KitNovember 12, 2025
K230623KITE Distal Fibula KitSeptember 1, 2023
K201147Elos® Intramedullary Nailing SystemJuly 19, 2021