Medical Device Manufacturer · US , Mchenry , IL

Codman & Shurtleff, Inc. - FDA 510(k) Cleared Devices

152 submissions · 151 cleared · Since 1976

Recent clearances: CERENOVUS Large Bore Catheter, CERENOVUS Large Bore Catheter, CereLink ICP Sensor Basic Kit, CereLink ICP Sensor Metal Skull Bolt Kit, CereLink ICP Sensor Plastic Skull Bolt Kit, CereLink ICP Sensor Ventricular Catheter Kit

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) Regulatory Record - Codman & Shurtleff, Inc.

152 devices
1-12 of 152

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