FDA 510(k) Application Details - K002423

Device Classification Name	Screw, Fixation, Intraosseous   More FDA Info for this Device
510(K) Number	K002423
Device Name	Screw, Fixation, Intraosseous
Applicant	BIOMET, INC. 56 EAST BELL DR. WARSAW, IN 46581-0587 US Other 510(k) Applications for this Company
Contact	TRACY BICKEL Other 510(k) Applications for this Contact
Regulation Number	872.4880   More FDA Info for this Regulation Number
Classification Product Code	DZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/08/2000
Decision Date	10/20/2000
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