FDA 510(k) Application Details - K024022

Device Classification Name	Applier, Cerclage   More FDA Info for this Device
510(K) Number	K024022
Device Name	Applier, Cerclage
Applicant	BIOMET, INC. 56 EAST BELL DR. WARSAW, IN 46581-0587 US Other 510(k) Applications for this Company
Contact	KACY ARNOLD Other 510(k) Applications for this Contact
Regulation Number	888.4540   More FDA Info for this Regulation Number
Classification Product Code	HXN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2002
Decision Date	01/23/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review