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

FDA 510(k) Regulatory Record - Codman & Shurtleff, Inc. Gastroenterology & Urology ✕

5 devices

1-5 of 5

Cleared Mar 23, 1993

CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)

Gastroenterology & Urology · 386d

Cleared Sep 29, 1989

DENVER PERITONEO-VENUS SHUNT

Gastroenterology & Urology · 64d

Cleared Jun 20, 1988

DENVER PLEURO-PERITONEAL SHUNT

Gastroenterology & Urology · 131d

Cleared May 31, 1988

DENVER PERITONEO-VENOUS SHUNT

Gastroenterology & Urology · 123d

Cleared Aug 25, 1987

CODMAN FLEXIBLE ENDOSCOPE

Gastroenterology & Urology · 95d