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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