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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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