Medical Device Manufacturer · US , Herndon , VA

Angiotech - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 2007

7

Total

6

Cleared

1

Denied

FDA 510(k) Regulatory Record - Angiotech General & Plastic Surgery ✕

4 devices

1-4 of 4

Cleared Sep 10, 2015

Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design

General & Plastic Surgery · 135d

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