FDA 510(k) Applications Submitted by ANGIOTECH

FDA 510(k) Number Submission Date Device Name Applicant
K151112 04/28/2015 Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design ANGIOTECH
K120827 03/19/2012 QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE) ANGIOTECH
K113744 12/20/2011 QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE) ANGIOTECH
K113800 12/23/2011 QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE ANGIOTECH
K070610 03/05/2007 SKATER BILIARY CATHETER ANGIOTECH
DEN090007 04/17/2009 BIO-SEAL LUNG BIOPSY TRACT SYSTEM ANGIOTECH
K073672 12/27/2007 SKATER BILIARY CATHETER ANGIOTECH


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