Surgical Specialties Corp. Dba Angiotech is one of 5148 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Specialties Corp. Dba Angiotech - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Surgical Specialties Corp. Dba Angiotech has 7 FDA 510(k) cleared medical devices. Based in Reading, US.
Historical record: 7 cleared submissions from 2012 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Specialties Corp. Dba Angiotech Filter by specialty or product code using the sidebar.
Surgical Specialties Corp. Dba Angiotech — FDA 510(k) Products and Clearance History
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