FDA 510(k), K181902, Codman Certas Plus Electronic Tool Kit

FDA 510(k), K181902, Codman Certas Plus Electronic Tool Kit

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510(K) Number: K181902
Device Name: Codman Certas Plus Electronic Tool Kit
Manufacturer: Nancy MacDonald
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: JXG
Classification Product Code: 07/16/2018
Date Received: 10/25/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology

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