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Coligne AG
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0
Known Names
coligne, co-ligne
Recent 510(k) Clearances
K-Number
Device
Date
K210306
GII Spinal Fixation System
May 19, 2021
K181963
ostaPek Interbody Fusion Cages
November 14, 2018
K173893
Trabis
September 6, 2018
K173148
ACIF
December 1, 2017