FDA 510(k) Application Details - K100724

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K100724
Device Name	Implant, Endosseous, Root-Form
Applicant	BIOMET 3I, INC. 4555 RIVERSIDE DR. PALM BEACH GARDENS, FL 33410 US Other 510(k) Applications for this Company
Contact	JOSE E CABRERA 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	03/15/2010
Decision Date	04/01/2011
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