Angiotech

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151112Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop DesignSeptember 10, 2015
DEN090007BIO-SEAL LUNG BIOPSY TRACT SYSTEMDecember 19, 2012
K120827QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)July 13, 2012
K113744QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)February 1, 2012
K113800QUILL QUADRAHELIX TISSUE-CLOSURE DEVICEJanuary 20, 2012
K073672SKATER BILIARY CATHETERJanuary 24, 2008
K070610SKATER BILIARY CATHETERJune 21, 2007