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FDA 510(k) Application Details - K010185
Device Classification Name
Implant, Endosseous, Root-Form
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510(K) Number
K010185
Device Name
Implant, Endosseous, Root-Form
Applicant
BICON, INC.
123 MORTON ST., 2ND FL.
BOSTON, MA 02130 US
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Contact
VINCENT J MORGAN
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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
01/19/2001
Decision Date
12/30/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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