FDA 510(k) Applications Submitted by MEDARTIS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K050934 04/14/2005 MODUS TITANIUM OSTEOSYNTHESIS SYSTEM MEDARTIS, INC.
K051567 06/14/2005 APTUS TITANIUM OSTEOSYNTHESIS SYSTEM MEDARTIS, INC.
K051946 07/18/2005 MODUS MODULAR DISTRACTION OSTEOGENESIS SYSTEM MEDARTIS, INC.
K052061 07/29/2005 MODUS IMF SCREWS 2.0 MEDARTIS, INC.


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