Integra Neurosciences Implants S.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integra Neurosciences Implants S.A. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Integra Neurosciences Implants S.A. has 6 FDA 510(k) cleared medical devices. Based in Planisboro, US.
Historical record: 6 cleared submissions from 2003 to 2008. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Integra Neurosciences Implants S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Integra Neurosciences Implants S.A.
6 devices
Cleared
Nov 06, 2008
OSV II
Neurology
136d
Cleared
Oct 06, 2004
EQUI-FLOW VALVE AND SHUNT SYSTEM
Neurology
15d
Cleared
Sep 02, 2004
LOW FLOW OSV II HYDROCEPHALUS VALVE
Neurology
21d
Cleared
Feb 26, 2004
MODIFICATION TO BURR HOLE VALVE AND SHUNT SYSTEM
Neurology
28d
Cleared
Dec 17, 2003
CONTOUR-FLEX VALVE AND SHUNT SYSTEM
Neurology
22d
Cleared
Oct 06, 2003
EXTERNAL DRAINAGE SET
Neurology
26d