Micro Surgical Instruments Corp. - FDA 510(k) Cleared Devices
15
Total
13
Cleared
0
Denied
Micro Surgical Instruments Corp. has 13 FDA 510(k) cleared medical devices. Based in Valencia, US.
Historical record: 13 cleared submissions from 1989 to 1994. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Micro Surgical Instruments Corp. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Jan 28, 1994
SERIES 5000 BATTERY POWERED INSTRUMENT SYSTEM
Orthopedic
315d
Cleared
Oct 05, 1993
IMPLANTOLOGY MODULE, MODEL 2175
Dental
134d
Cleared
Aug 02, 1993
ELECTRIC WIRE DRIVER, MODEL 2640E
Orthopedic
199d
Cleared
Jun 02, 1992
MICROAIRE(R) FACIAL BONE PLATING SYSTEM
Orthopedic
208d
Cleared
Feb 05, 1992
MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE
Orthopedic
84d
Cleared
Nov 27, 1991
DRILL MODULES MODELS 2116/2117
Ear, Nose, Throat
61d
Cleared
Nov 01, 1991
MICRO-AIRE MODEL 2060
General & Plastic Surgery
95d
Cleared
Oct 21, 1991
MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS
General & Plastic Surgery
90d
Cleared
Jun 21, 1991
FIXATION DEVICES AND BONE PLATE
Orthopedic
157d
Cleared
Jun 18, 1991
2710-000 OSCILLATING SAW, GENERAL ASSEMBLY
General & Plastic Surgery
201d
Cleared
Jan 22, 1991
MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESS
Physical Medicine
63d
Cleared
Jan 08, 1991
MICRO-AIRE 4220-000 OSCILLATING SAW
Orthopedic
46d