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FDA 510(k) Application Details - K020667
Device Classification Name
Shunt, Central Nervous System And Components
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510(K) Number
K020667
Device Name
Shunt, Central Nervous System And Components
Applicant
Codman & Shurtleff, Inc.
325 PARAMOUNT DR.
RAYNHAM, MA 02767-0350 US
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Contact
ELIZABETH DOLAN
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Regulation Number
882.5550
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Classification Product Code
JXG
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More FDA Info for this Product Code
Date Received
03/01/2002
Decision Date
03/28/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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