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FDA 510(k) Applications Submitted by Medos International S└RL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K223688
12/09/2022
CONDUITÖ Lateral Lumbar Intervertebral Fusion Cage, CONDUITÖ Instruments
Medos International S└RL
K231527
05/26/2023
TriALTIS Navigation Enabled Instruments
Medos International S└RL
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