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Pipeline Orthopedics

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K131368NEO KNEE SYSTEMOctober 3, 2013
K132046PIPELINE KNEE SYSTEMSeptember 23, 2013
K130353PIPELINE TOTAL HIP SYSTEM (LINE EXTENSION)July 1, 2013
K131237PIPELINE TOTAL HIP SYSTEMJune 13, 2013
K123692PIPELINE KNEE SYSTEMMay 24, 2013
K122500NEO PS KNEE SYSTEMMay 3, 2013
K120313NEO CR KNEE SYSTEMApril 20, 2012
K113122PIPELINE CR PRIMARY KNEE SYSTEMMarch 20, 2012
K112802PIPELINE TOTAL HIP SYSTEMMarch 9, 2012