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

FDA 510(k) Number Applicant Device Name Decision Date
K123128 ALLERGAN SERI SURGICAL SCAFFOLD 04/25/2013
K172545 Sofregen Medical, Inc. SERI Contour 09/22/2017
K163217 W. L. GORE & ASSOCIATES, INC. GORE BIO-A Tissue Reinforcement 02/10/2017
K222919 W. L. Gore and Associates, Inc. GORE« ENFORM Biomaterial 12/19/2022
K173333 W.L. Gore & Associates, Inc. GORE ENFORM Biomaterial 04/05/2018


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