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
FDA 510(k) Regulatory Record - Angiotech Anesthesiology ✕
1 devices