T. Korossurgical Instruments Corp. - FDA 510(k) Cleared Devices
27
Total
24
Cleared
0
Denied
T. Korossurgical Instruments Corp. has 24 FDA 510(k) cleared medical devices. Based in Westlake, US.
Historical record: 24 cleared submissions from 1985 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by T. Korossurgical Instruments Corp. Filter by specialty or product code using the sidebar.
27 devices
Cleared
Apr 27, 2001
GRAFT MARKER RING
Cardiovascular
308d
Cleared
Dec 04, 2000
NON-ABSORBING STERNATOMY MONOFILAMENT SUTURE
Orthopedic
90d
Cleared
Jan 25, 1996
VIDEOSCOPE W/IRRIGATION SHEATH
Orthopedic
153d
Cleared
Dec 04, 1995
DISCETOME TISSUE ASPIRATOR
Orthopedic
102d
Cleared
Nov 06, 1995
PERCUTANEOUS DISCECTOMY CANNULA SYSTEM
Orthopedic
73d
Cleared
Nov 06, 1995
ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES
Orthopedic
69d
Cleared
Mar 22, 1994
CERVICAL SELF-RETAINING RETRACTOR
Neurology
126d
Cleared
Aug 06, 1993
REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR
General & Plastic Surgery
322d
Cleared
Aug 06, 1993
THOROCOSCOPY SELF-RETAINING RETRACTOR
General & Plastic Surgery
322d
Cleared
Aug 06, 1993
REUSABLE/INTERCHANGEABLE SHAFT, ENDOSCOPIC SCISSOR
General & Plastic Surgery
151d
Cleared
Jun 08, 1993
ENDOSCOPIC OR THORASCOPIC FORCEPS
General & Plastic Surgery
88d
Cleared
May 17, 1993
UNIVERSAL SURGICAL INSTRUMENT HOLDER
General & Plastic Surgery
241d