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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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