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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Shunt, Central Nervous System And Components
510(k) Number K172022
Device Name CODMAN Hydrocephalus Valves, Catheters & Accessories (Bundled)
Applicant
Codman & Shurtleff, Inc.
325 Paramount Drive
Raynham,  MA  02767
Applicant Contact Christopher Garete
Correspondent
Codman & Shurtleff, Inc.
325 Paramount Drive
Raynham,  MA  02767
Correspondent Contact Christopher Garete
Regulation Number882.5550
Classification Product Code
JXG  
Date Received07/05/2017
Decision Date 10/03/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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