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FDA 510(k) Application Details - K023079
Device Classification Name
Crown And Bridge, Temporary, Resin
More FDA Info for this Device
510(K) Number
K023079
Device Name
Crown And Bridge, Temporary, Resin
Applicant
ANAXDENT GMBH
1730 PENNSYLVANIA N.W.
WASHINGTON, DC 20006 US
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Contact
DVORAH RICHMAN
Other 510(k) Applications for this Contact
Regulation Number
872.3770
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Classification Product Code
EBG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/16/2002
Decision Date
10/30/2002
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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