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FDA 510(k) Applications Submitted by SI-Technology, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K251525
05/19/2025
SI-TECHNOLOGY« SI-DESIS« XÖ Sacroiliac Joint Fusion System
SI-Technology, LLC
K151462
06/01/2015
SI-TECHNOLOGY« SI-DESIS« SCREWS
SI-TECHNOLOGY, LLC
K241813
06/21/2024
SI-TECHNOLOGY« SI-DESIS« XÖ Sacroiliac Joint Fusion System
SI-Technology, LLC
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