FDA 510(k) Application Details - K002614

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K002614
Device Name	Implant, Endosseous, Root-Form
Applicant	CORE-VENT CORP. 4630 SOUTH ARVILLE STE D LAS VEGAS, NV 89103 US Other 510(k) Applications for this Company
Contact	WILL FISHER Other 510(k) Applications for this Contact
Regulation Number	872.3640   More FDA Info for this Regulation Number
Classification Product Code	DZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/22/2000
Decision Date	12/08/2000
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