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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
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