FDA 510(k) Application Details - K961383

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K961383
Device Name	Implant, Endosseous, Root-Form
Applicant	THE EMERGING TECHNOLOGIES GROUP 824 U.S. HWY. 1, SUITE 370 NORTH PALM BEACH, FL 33408 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	03/19/1996
Decision Date	09/25/1996
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