CODMAN HAKIM SHUNT SYSTEMS

Shunt, Central Nervous System And Components

Codman & Shurtleff, Inc.

The following data is part of a premarket notification filed by Codman & Shurtleff, Inc. with the FDA for Codman Hakim Shunt Systems.

Pre-market Notification Details

Device IDK020667
510k NumberK020667
Device Name:CODMAN HAKIM SHUNT SYSTEMS
ClassificationShunt, Central Nervous System And Components
Applicant Codman & Shurtleff, Inc. 325 PARAMOUNT DR. Raynham,  MA  02767 -0350
ContactElizabeth Dolan
CorrespondentElizabeth Dolan
Codman & Shurtleff, Inc. 325 PARAMOUNT DR. Raynham,  MA  02767 -0350
Product CodeJXG  
CFR Regulation Number882.5550 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-03-01
Decision Date2002-03-28
Summary:summary

NIH GUDID Devices

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