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FDA 510(k) Application Details - K990660
Device Classification Name
Shunt, Central Nervous System And Components
More FDA Info for this Device
510(K) Number
K990660
Device Name
Shunt, Central Nervous System And Components
Applicant
NMT NEUROSCIENCES IMPLANTS S.A.
6011 CELLINI ST.
CORAL GABLES, FL 33146 US
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Contact
BARBARA RAMSEYER
Other 510(k) Applications for this Contact
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
03/01/1999
Decision Date
09/23/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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