FDA 510(k) Application Details - K001114

Device Classification Name	Crown And Bridge, Temporary, Resin   More FDA Info for this Device
510(K) Number	K001114
Device Name	Crown And Bridge, Temporary, Resin
Applicant	3M COMPANY 3M CENTER BLDG. 275-3SE-08 ST. PAUL, MN 55144-1000 US Other 510(k) Applications for this Company
Contact	CHERI SMOKOVICH Other 510(k) Applications for this Contact
Regulation Number	872.3770   More FDA Info for this Regulation Number
Classification Product Code	EBG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/06/2000
Decision Date	06/09/2000
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