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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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