Surgical Specialties Corp. Dba Angiotech
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K133420 | TRANQUILL BARBED DEVICE | NEW | 2013-11-29 | View |
| 510(k) | K131224 | SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE | GAW | 2013-05-16 | View |
| 510(k) | K130078 | QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN | GAW | 2013-02-28 | View |
| 510(k) | K123877 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN | NEW | 2013-01-02 | View |
| 510(k) | K123836 | QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN | GAM | 2012-12-21 | View |
| 510(k) | K123409 | QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN | GAM | 2012-11-20 | View |
| 510(k) | K122898 | QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN | GAM | 2012-10-22 | View |
No matching devices.
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