FDA 510(k), K103787, MEDEOR MATRIX
FDA 510(k), K103787, MEDEOR MATRIX
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510(K) Number: K103787
Device Name: MEDEOR MATRIX
Manufacturer: KENSEY NASH CORP.
Device Classification Name: mesh, surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 12/27/2010
Decision Date: 02/07/2011
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MEDEOR MATRIX
Manufacturer: KENSEY NASH CORP.
Device Classification Name: mesh, surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 12/27/2010
Decision Date: 02/07/2011
Regulation Medical Specialty: General & Plastic Surgery