FDA 510(k) Applications Submitted by PIPELINE ORTHOPEDICS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120313	02/01/2012	NEO CR KNEE SYSTEM	PIPELINE ORTHOPEDICS
K130353	02/12/2013	PIPELINE TOTAL HIP SYSTEM (LINE EXTENSION)	PIPELINE ORTHOPEDICS
K131237	05/01/2013	PIPELINE TOTAL HIP SYSTEM	PIPELINE ORTHOPEDICS
K131368	05/13/2013	NEO KNEE SYSTEM	PIPELINE ORTHOPEDICS
K132046	07/02/2013	PIPELINE KNEE SYSTEM	PIPELINE ORTHOPEDICS
K122500	08/16/2012	NEO PS KNEE SYSTEM	PIPELINE ORTHOPEDICS
K112802	09/27/2011	PIPELINE TOTAL HIP SYSTEM	PIPELINE ORTHOPEDICS
K113122	10/21/2011	PIPELINE CR PRIMARY KNEE SYSTEM	PIPELINE ORTHOPEDICS
K123692	12/03/2012	PIPELINE KNEE SYSTEM	PIPELINE ORTHOPEDICS