Codman & Shurtleff, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Codman & Shurtleff, Inc. - FDA 510(k) Cleared Devices
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
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.
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