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FDA 510(k) Applications Submitted by KIMBERLY L PRUITT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032371
08/01/2003
TITANIUM MESH SYSTEM
ENCORE MEDICAL, L.P.
K032905
09/17/2003
3DKNEE POROUS COATED FEMORAL COMPONENT
ENCORE ORTHOPEDICS, INC.
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