Surgical Specialties Corp - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Surgical Specialties Corp has 22 FDA 510(k) cleared general & plastic surgery devices. Based in Reading, US.
Historical record: 22 cleared submissions from 2000 to 2014.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
22 devices
Cleared
Jul 18, 2014
POLYSYN SURGICAL SUTURE
General & Plastic Surgery
31d
Cleared
Jul 11, 2014
QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE
General & Plastic Surgery
29d
Cleared
Feb 28, 2014
MONODERM SURGICAL SUTURE
General & Plastic Surgery
29d
Cleared
Apr 23, 2008
QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF POLYDIOXANONE (PDO)
General & Plastic Surgery
16d
Cleared
Mar 21, 2008
QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF PDO (POLYDIOXANONE
General & Plastic Surgery
11d
Cleared
Aug 06, 2007
QUILL SELF-RETAINING SYSTEM (SRS) SYNTHETIC ABSORBABLE SURGICAL SUTURE MATERIAL
General & Plastic Surgery
17d
Cleared
Aug 03, 2007
QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF MONODERM
General & Plastic Surgery
10d
Cleared
May 09, 2007
SHARPOINT PDO (POLYDIOXANONE) SUTURES
General & Plastic Surgery
149d
Cleared
Jan 18, 2006
CONTOUR THREAD SYNTHETIC ABSORBABLE PDO BARBED SUTURE
General & Plastic Surgery
44d
Cleared
Dec 06, 2005
OPTIMIZED BARB DESIGN
General & Plastic Surgery
46d
Cleared
Nov 07, 2005
MODIFIED MONODERM MONOFILAMENT, SYNTHETIC, ABSORBABLE SUTURE
General & Plastic Surgery
62d
Cleared
Apr 01, 2005
CONTOUR MIDFACE OPPOSING UNI-DIRECTIONAL THREADS
General & Plastic Surgery
30d