FDA 510(k) Applications Submitted by TATYANA KORSUNSKY

FDA 510(k) Number Submission Date Device Name Applicant
K130912 04/02/2013 OMNICUT RESECTION BLADE DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K171237 04/27/2017 FMS VUE II Fluid Management and Tissue Debridement System Medos International SARL
K181182 05/03/2018 DYNACORD Suture Medos International SARL
K181809 07/06/2018 GRYPHON« Anchors with DYNACORDÖ Suture Medos International SARL
K162247 08/10/2016 PERMATAPE MEDOS INTERNATIONAL SARL
K123668 11/29/2012 ORTHOCORD DEPUY MITEK INC., A JOHNSON AND JOHNSON COMPANY
K133794 12/13/2013 4.5MM HEALIX ADVANCE BR ANCHOR, WITH 2 OR 3 STRANDS OF #2 PERMACORD SUTURE, 5.5MM HEALIX ADVANCE BR ANCHOR, WITH 2 OR 3 DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K173859 12/20/2017 HEALIX ADVANCE Anchor with DYNACORD Suture Medos International SARL


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