FDA 510(k) Applications Submitted by John Brunelle, Ph.D.

FDA 510(k) Number Submission Date Device Name Applicant
K240458 02/16/2024 Synthetic Bone Putty Ventris Medical
K160446 02/17/2016 MCP Bone Putty BioStructures, LLC
K250556 02/25/2025 Porous Biologic Scaffold Ventris Medical
K240765 03/20/2024 Porous Biologic Scaffold Ventris Medical
K221644 06/06/2022 Synthetic Bone Putty Ventris Medical
K162860 10/12/2016 MCS Bone Graft BIOVENTUS LLC
K142276 08/15/2014 MCS Bone Graft BIOSTRUCTURES, LLC


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