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FDA 510(k) Application Details - K031345
Device Classification Name
Implant, Endosseous, Root-Form
More FDA Info for this Device
510(K) Number
K031345
Device Name
Implant, Endosseous, Root-Form
Applicant
NOBEL BIOCARE UAS INC
22715 SAVI RANCH PKWY.
YORBA LINDA, CA 92887 US
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Contact
ELIZABETH J MASON
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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
04/29/2003
Decision Date
07/24/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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