FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LICOX PMO BRAIN MONITORING SYSTEM

K Number: K040235 · Decision Apr 20, 2004
Classifications
1
FEI Numbers
63
Registration Numbers
64
Same Product Code
102
Applicant Total
42
Review Days
78

Basic Information

Device Name
LICOX PMO BRAIN MONITORING SYSTEM
K Number
K040235
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1620
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
INTEGRA LIFESCIENCES CORPORATION
Date Received
February 2, 2004
Decision Date
April 20, 2004
Product Code
GWM
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWM Device, Monitoring, Intracranial Pressure

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWM), ordered by most recent decision date.

View all

Other Clearances by INTEGRA LIFESCIENCES CORPORATION

K Number Device Name
K163456 DuraGen Secure Dural Regeneration Matrix
K160811 CRW STEREOTACTIC SYSTEM
K161882 CUSA Clarity Ultrasonic Surgical Aspirator System
K161992 Horizontal-Vertical Lumbar Valve Systems, Spetzler Lumbar Peritoneal Shunt Systems
K161189 Integra TITAN Reverse Shoulder System
K153041 Bundled Neurological Shunts and Accessories Product Families Labeling Modification to Support MR Conditional Labeling
K152897 Integra DP Valve Systems (including Burr Hole Reservoirs and Stainless Steel Connectors), Gravity Compensating Accessory
K140722 INTEGRA FLOW REGULATING VALVE SYSTEMS OSV II MODELS AND INTEGRA FLOW REGULATING VALVE LOW FLOW MODELS
K142238 MAYFIELD Skull Clamp
K141674 CUSA EXCEL+ ULTRASONIC SURGICAL ASPIRATOR SYSTEM
Search all 42 clearances from INTEGRA LIFESCIENCES CORPORATION →