FDA 510(k) Application Details - K760961

Device Classification Name Clip, Aneurysm

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510(K) Number K760961
Device Name Clip, Aneurysm
Applicant CODMAN & SHURTLEFF, INC.

, US
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Regulation Number 882.5200

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Classification Product Code HCH
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Date Received 10/29/1976
Decision Date 11/12/1976
Decision SE - Substantially Equivalent
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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