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FDA 510(k) Application Details - K023336
Device Classification Name
Implant, Endosseous, Root-Form
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510(K) Number
K023336
Device Name
Implant, Endosseous, Root-Form
Applicant
"O" CO., INC.
600 PAISANO, N.E., SUITE A
ALBUQUERQUE, NM 87123 US
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Contact
DAVID D DALISE
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Regulation Number
872.3640
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Classification Product Code
DZE
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More FDA Info for this Product Code
Date Received
10/07/2002
Decision Date
10/09/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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