FDA 510(k), K053656, TYRX ANTIMICROBIAL MESH
FDA 510(k), K053656, TYRX ANTIMICROBIAL MESH
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510(K) Number: K053656
Device Name: TYRX ANTIMICROBIAL MESH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 12/30/2005
Decision Date: 07/14/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TYRX ANTIMICROBIAL MESH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 12/30/2005
Decision Date: 07/14/2006
Regulation Medical Specialty: General & Plastic Surgery