Company ยท US
Angiotech
FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2015. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 10, 2015 | K151112 | Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design Angiotech | GAW |
| Dec 19, 2012 | DEN090007 | BIO-SEAL LUNG BIOPSY TRACT SYSTEM Angiotech, CA | OMT |
| Jul 13, 2012 | K120827 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE) Angiotech | NEW |
| Feb 1, 2012 | K113744 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE) Angiotech | NEW |
| Jan 20, 2012 | K113800 | QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE Angiotech | GAW |
| Jan 24, 2008 | K073672 | SKATER BILIARY CATHETER Angiotech | FGE |
| Jun 21, 2007 | K070610 | SKATER BILIARY CATHETER Angiotech | FGE |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||