FDA 510(k) Application Details - K960371

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K960371
Device Name	Implant, Endosseous, Root-Form
Applicant	INTERPORE INTL. 181 TECHNOLOGY DR. IRVINE, CA 92618-2402 US Other 510(k) Applications for this Company
Contact	DAVID P BALDING 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	01/26/1996
Decision Date	03/08/1996
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