Surgical Specialties Corp. Dba Angiotech - FDA 510(k) Cleared Devices
Recent clearances: TRANQUILL BARBED DEVICE, SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgical Specialties Corp. Dba Angiotech General & Plastic Surgery ✕
7 devices
Cleared
Nov 29, 2013
TRANQUILL BARBED DEVICE
General & Plastic Surgery
21d
Cleared
May 16, 2013
SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE,...
General & Plastic Surgery
16d
Cleared
Feb 28, 2013
QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
General & Plastic Surgery
45d
Cleared
Jan 02, 2013
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
General & Plastic Surgery
16d
Cleared
Dec 21, 2012
QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
General & Plastic Surgery
8d
Cleared
Nov 20, 2012
QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
General & Plastic Surgery
15d
Cleared
Oct 22, 2012
QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
General & Plastic Surgery
31d