Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Angiotech

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K120827 QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)NEW2012-07-13 View
510(k) K113744 QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)NEW2012-02-01 View
510(k) K113800 QUILL QUADRAHELIX TISSUE-CLOSURE DEVICEGAW2012-01-20 View
510(k) K073672 SKATER BILIARY CATHETERFGE2008-01-24 View
510(k) K070610 SKATER BILIARY CATHETERFGE2007-06-21 View
↑