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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