Codman & Shurtleff, Inc. - FDA 510(k) Cleared Devices
152
Total
151
Cleared
0
Denied
Codman & Shurtleff, Inc. has 151 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 151 cleared submissions from 1976 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Codman & Shurtleff, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Codman & Shurtleff, Inc.
152 devices
Cleared
Jul 20, 2020
CERENOVUS Large Bore Catheter
Neurology
228d
Cleared
Nov 08, 2019
CERENOVUS Large Bore Catheter
Neurology
184d
Cleared
Nov 08, 2017
CereLink ICP Sensor Basic Kit, CereLink ICP Sensor Metal Skull Bolt Kit,...
Neurology
37d
Cleared
Oct 16, 2017
Codman EDS 3 CSF External Drainage System, Codman EDS 3 CSF External Drainage...
Neurology
55d
Cleared
Oct 03, 2017
CODMAN Hydrocephalus Valves, Catheters & Accessories (Bundled)
Neurology
90d
Cleared
Sep 25, 2017
GALAXY G3 Mini Microcoil Delivery System
Neurology
95d
Cleared
Jul 14, 2017
MICRUSFRAME 10 Stretch Resistant Microcoil Delivery System, MICRUSFRAME 18...
Neurology
31d
Cleared
Jul 03, 2017
YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up
Cardiovascular
28d
Cleared
Jan 05, 2017
YOGA Microcatheter
Cardiovascular
113d
Cleared
Oct 28, 2016
Codman EDS3 CSF External Drainage System
Neurology
58d
Cleared
Aug 19, 2016
Codman Microsensor Basic Kit, Codman Microsensor Plastic Skull Bolt Kit,...
Neurology
273d
Cleared
Oct 30, 2015
DURAFORM Dural Graft Implant
Neurology
60d
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