FDA 510(k) Application Details - K955428

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K955428
Device Name	Implant, Endosseous, Root-Form
Applicant	IMPLANT INNOVATIONS, INC. 3071 CONTINENTAL DR. WEST PALM BEACH, FL 33407 US Other 510(k) Applications for this Company
Contact	WILLIAM G CONETY 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	11/28/1995
Decision Date	02/08/1996
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