FDA 510(k) Applications Submitted by Prosidyan, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K143533 12/12/2014 FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE PROSIDYAN, INC.
K241426 05/20/2024 GPS Advanced; 5 cc GPS Advanced Cannula Prosidyan, Inc.
K251648 05/29/2025 GPS Advanced; GPS Advanced Cannula Prosidyan, Inc.


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