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FDA 510(k) Applications Submitted by REBECCA LENNARD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062352
08/11/2006
FRS SCREW
DEPUY ORTHOPAEDICS, INC.
K063652
12/08/2006
GLOBAL AP POROUS COATED HUMERAL STEM
DEPUY ORTHOPAEDICS, INC.
K063686
12/12/2006
DEPUY LPS DISTAL FEMORAL COMPONENT
DEPUY ORTHOPAEDICS, INC.
K040644
03/11/2004
MODIFICATION TO DEPUY CERAMIC FEMORAL HEAD
DEPUY ORTHOPAEDICS, INC.
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