Neuro Navigational Corp. - FDA 510(k) Cleared Devices
23
Total
21
Cleared
0
Denied
Neuro Navigational Corp. has 21 FDA 510(k) cleared medical devices. Based in Costa Mesa, US.
Historical record: 21 cleared submissions from 1993 to 1997. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuro Navigational Corp. Filter by specialty or product code using the sidebar.
23 devices
Cleared
Mar 06, 1997
2.1MM SEMI-RIGID NEUROVIEW SCISSORS/2.0OMM SEMI-RIGID NEUROVIEW GRASPING FORCEPS
Neurology
77d
Cleared
Jun 13, 1996
NEUROVIEW SCISSORS
Neurology
63d
Cleared
Jun 07, 1996
1.2MM REUSABLE NEUROVIEW ENDOSCOPE
Neurology
74d
Cleared
Jun 07, 1996
ASPIRATION/IRRIGATION CATHETER
Neurology
64d
Cleared
Apr 11, 1996
DISPOSABLE NEUROVIEW INTRODUCER SHEATH
Neurology
44d
Cleared
Mar 07, 1996
DISPOSABLE NEUROVIEW OPERATING SHEATH
Neurology
129d
Cleared
Feb 29, 1996
NEUROVIEW COAXIAL BIPOLAR ELECTRODE
Neurology
100d
Cleared
Dec 19, 1995
RIGID NEUROVIEW ENDOSCOPE
Neurology
55d
Cleared
Dec 18, 1995
NEUROVIEW COAXIAL BIPOLAR ELECTRODE
General & Plastic Surgery
18d
Cleared
Dec 04, 1995
RIGID NEUROVIEW ENDOSCOPE
Orthopedic
31d
Cleared
Sep 08, 1995
DISPOSABLE BIOPSY FORCEP
Orthopedic
92d
Cleared
Sep 08, 1995
DISPOSABLE TOOTHED GRASPING FORCEP
Orthopedic
91d