Integra Neurosciences is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integra Neurosciences - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Integra Neurosciences has 8 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 8 cleared submissions from 2000 to 2008. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Integra Neurosciences Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Integra Neurosciences
8 devices
Cleared
Oct 10, 2008
AURAGEN CORTICAL SURFACE ELECTRODES
Neurology
63d
Cleared
May 11, 2005
NEUROSENSOR CEREBRAL BLOOD FLOW AND INTRACRANIAL PRESSURE MONITORING...
Neurology
51d
Cleared
May 14, 2003
CAMINO SINGLE PARAMETER MONITOR, MODEL SPM-1
Neurology
37d
Cleared
Sep 13, 2002
SELECTOR INTEGRA ULTRASONIC SURGICAL ASPIRATOR, MODEL OM 1530000M3
General & Plastic Surgery
87d
Cleared
Aug 23, 2002
MONITORR ICP EXTERNAL CSF DRAINAGE AND MONITORING SYSTEM
Neurology
21d
Cleared
Aug 20, 2002
CAMINO INTRACRANIAL PRESSURE MONITORING CATHETER WITH LICOX IMC BOLT FITTING,...
Neurology
18d
Cleared
Mar 21, 2002
LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE
Neurology
29d
Cleared
Nov 24, 2000
LICOX CMP MONITOR-AC3.1, LICOX IMC OXYGEN CATHETERS-CC1,CC1.SB LUICOX IMC...
Neurology
80d