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FDA 510(k) Applications Submitted by GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050473
02/24/2005
RBK PATELLA FEMORAL KNEE
GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K051721
06/27/2005
GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM
GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K033351
10/20/2003
GLOBAL RESURFACING UNICOMPARTMENTAL (GRU) KNEE
GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
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