FDA 510(k) Application Details - K150501

Device Classification Name	Prosthesis, Elbow, Constrained, Cemented   More FDA Info for this Device
510(K) Number	K150501
Device Name	Prosthesis, Elbow, Constrained, Cemented
Applicant	ZIMMER, INC. P.O. BOX 708 WARSAW, IN 46580-0708 US Other 510(k) Applications for this Company
Contact	Keith Proctor Other 510(k) Applications for this Contact
Regulation Number	888.3150   More FDA Info for this Regulation Number
Classification Product Code	JDC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/26/2015
Decision Date	04/23/2015
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