FDA 510(k) Application Details - K123907

Device Classification Name	Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer   More FDA Info for this Device
510(K) Number	K123907
Device Name	Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
Applicant	BIOMET MANUFACTURING CORP. 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	888.3540   More FDA Info for this Regulation Number
Classification Product Code	KRR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/19/2012
Decision Date	09/03/2013
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