FDA 510(k) Applications Submitted by PROSIDYAN, INC

FDA 510(k) Number Submission Date Device Name Applicant
K180080 01/10/2018 FIBERGRAFT BG Matrix Bone Graft Substitute Prosidyan, Inc
K170306 01/31/2017 FIBERGRAFT BG Putty Bone Graft Substitute Prosidyan, Inc
K171284 05/01/2017 FIBERGRAFT BG Matrix Bone Graft Substitute Prosidyan, Inc
K182670 09/25/2018 FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute Prosidyan, Inc
K213803 12/06/2021 FIBERGRAFT Aeridyan Matrix Bone Graft Substitute Prosidyan, Inc
K141956 07/18/2014 FIBERGRAFT BG MORSELS PROSIDYAN, INC
K132805 09/06/2013 BG MORSELS PROSIDYAN, INC


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact