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FDA 510(k) Application Details - K070568
Device Classification Name
Implant, Endosseous, Root-Form
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510(K) Number
K070568
Device Name
Implant, Endosseous, Root-Form
Applicant
DIO DEPARTMENT DSI, INC.
13340 E. FIRESTONE BLVD
SUITE J
SANTA FE SPRINGS, CA 90670 US
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Contact
KENNY LIM
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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
02/28/2007
Decision Date
05/25/2007
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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