FDA 510(k) Application Details - K983120

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K983120
Device Name	Implant, Endosseous, Root-Form
Applicant	ORALTRONICS MARKETING-UND VERTRIEBS GMBH 4329 GRAYDON RD. SAN DIEGO, CA 92130 US Other 510(k) Applications for this Company
Contact	FLOYD G LARSON 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	09/04/1998
Decision Date	07/29/1999
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