FDA 510(k) Application Details - K161233

Device Classification Name	Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous   More FDA Info for this Device
510(K) Number	K161233
Device Name	Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
Applicant	SMITH & NEPHEW, INC. 7135 GOODLETT FARMS PARKWAY CORDOVA, TN 38016 US Other 510(k) Applications for this Company
Contact	MIKE SCOTT Other 510(k) Applications for this Contact
Regulation Number	888.3358   More FDA Info for this Regulation Number
Classification Product Code	MBL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/02/2016
Decision Date	12/14/2016
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