FDA 510(k) Applications for Medical Device Product Code "OXE"

FDA 510(k) Number Applicant Device Name Decision Date
K170945 Cook Biotech Incorporated Biodesign Staple Line Reinforcement 04/28/2017
K022044 COOK BIOTECH, INC. SURGISIS STAPLE LINE REINFORCEMENT 08/23/2002
K153364 Kerecis Limited Kerecis SecureMesh 08/19/2016
K030879 SYNOVIS SURGICAL INNOVATIONS VERITAS COLLAGEN MATRIX 04/24/2003


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