FDA 510(k) Application Details - K952996

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K952996
Device Name	Implant, Endosseous, Root-Form
Applicant	IMPLANT CENTER OF THE PALM BEACHES 824 US HWY I, STE. 370 N. PALM BEACH, FL US Other 510(k) Applications for this Company
Contact	JACK T KRAUSER 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	06/23/1995
Decision Date	10/31/1995
Decision	SE - Substantially Equivalent
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review