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FDA 510(k) Applications Submitted by MANDY COE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090313
02/09/2009
PIGALILEO TKR BASE V2.3 AND CAS V4.1
SMITH & NEPHEW, INC.
K090982
04/07/2009
SMITH & NEPHEW HIP SYSTEMS WITH HA
SMITH & NEPHEW, INC.
K083762
12/18/2008
BIOLOX DELTA CERAMIC FEMORAL HEADS
SMITH & NEPHEW, INC.
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