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FDA 510(k) Applications Submitted by MERRIES INTERNATIONAL INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K051698
06/24/2005
MERRIES UNI-OSTEO, MODEL CS30250-CS10102
MERRIES INTERNATIONAL INC.
K063157
10/17/2006
MERRIES K-PHATE BONE GRAFT SUBSTITUTE
MERRIES INTERNATIONAL INC.
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