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Depuy France S.A.S.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K173960
DePuy Corail AMT Hip Prosthesis
September 21, 2018
K123991
DEPUY CORAIL AMT HIP PROSTHESIS
September 16, 2013
K122442
DEPUY CTA REVERSE SHOULDER SYSTEM
September 6, 2012
K120174
DEPUT DELTA XTEND REVERSE SHOULDER
June 11, 2012