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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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