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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