FDA 510(k), K091499, MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)
FDA 510(k), K091499, MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)
Device Name: MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)
Manufacturer:
Device Classification Name: Mesh, Surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 05/21/2009
Decision Date: 10/22/2009
Regulation Medical Specialty: General & Plastic Surgery
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