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FDA 510(k) Application Details - K970168
Device Classification Name
Crown And Bridge, Temporary, Resin
More FDA Info for this Device
510(K) Number
K970168
Device Name
Crown And Bridge, Temporary, Resin
Applicant
3M COMPANY
3M CENTER
BLDG. 275-3SE-08
ST. PAUL, MN 55144-1000 US
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Contact
ANY FOWLER
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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
01/16/1997
Decision Date
02/27/1997
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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