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FDA 510(k) Applications Submitted by JENIK RADON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050457
02/23/2005
MERETE METAFIX SMALL FRAGMENT BONE PLATE SYSTEM
MERETE MEDICAL GMBH
K050924
04/13/2005
MERETE DUOTHREADTM BONE SCREW
MERETE MEDICAL GMBH
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