Medical Device Manufacturer · US , Herndon , VA

Angiotech - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 2007
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
1-7 of 7
Cleared Sep 10, 2015
Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design
K151112 · GAW
General & Plastic Surgery · 135d
Not Cleared Dec 19, 2012
BIO-SEAL LUNG BIOPSY TRACT SYSTEM
DEN090007 · OMT
Anesthesiology · 1342d
Cleared Jul 13, 2012
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)
K120827 · NEW
General & Plastic Surgery · 116d
Cleared Feb 01, 2012
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)
K113744 · NEW
General & Plastic Surgery · 43d
Cleared Jan 20, 2012
QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE
K113800 · GAW
General & Plastic Surgery · 28d
Cleared Jan 24, 2008
SKATER BILIARY CATHETER
K073672 · FGE
Gastroenterology & Urology · 28d
Cleared Jun 21, 2007
SKATER BILIARY CATHETER
K070610 · FGE
Gastroenterology & Urology · 108d
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All7 General & Plastic Surgery 4 Gastroenterology & Urology 2 Anesthesiology 1