FDA 510(k) Application Details - K042466

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K042466
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	ZEST ANCHORS, INC. 2061 WINERIDGE PL., SUITE 100 ESCONDIDO, CA 92029 US Other 510(k) Applications for this Company
Contact	PAUL ZUEST Other 510(k) Applications for this Contact
Regulation Number	872.3630   More FDA Info for this Regulation Number
Classification Product Code	NHA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/13/2004
Decision Date	11/24/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review