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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