FDA 510(k) Application Details - K110039

Device Classification Name	Cerclage, Fixation   More FDA Info for this Device
510(K) Number	K110039
Device Name	Cerclage, Fixation
Applicant	BIOMET SPORTS MEDICINE 56 EAST BELL DRIVE P.O. BOX 587 WARSAW, IN 46581-0587 US Other 510(k) Applications for this Company
Contact	ELIZABETH WRAY Other 510(k) Applications for this Contact
Regulation Number	888.3010   More FDA Info for this Regulation Number
Classification Product Code	JDQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/06/2011
Decision Date	05/03/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review