Angiotech is one of 13005 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Angiotech - FDA 510(k) Cleared Devices
Recent clearances: Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design, QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE), QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)
7
Total
6
Cleared
1
Denied
Angiotech has 6 FDA 510(k) cleared medical devices. Based in Herndon, US.
Historical record: 6 cleared submissions from 2007 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Angiotech Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angiotech
7 devices
Cleared
Sep 10, 2015
Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design
General & Plastic Surgery
135d
Not Cleared
Dec 19, 2012
BIO-SEAL LUNG BIOPSY TRACT SYSTEM
Anesthesiology
1342d
Cleared
Jul 13, 2012
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)
General & Plastic Surgery
116d
Cleared
Feb 01, 2012
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)
General & Plastic Surgery
43d
Cleared
Jan 20, 2012
QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE
General & Plastic Surgery
28d
Cleared
Jan 24, 2008
SKATER BILIARY CATHETER
Gastroenterology & Urology
28d
Cleared
Jun 21, 2007
SKATER BILIARY CATHETER
Gastroenterology & Urology
108d