FDA 510(k), K061533, PROCEED VENTRAL PATCH
FDA 510(k), K061533, PROCEED VENTRAL PATCH
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510(K) Number: K061533
Device Name: PROCEED VENTRAL PATCH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 06/02/2006
Decision Date: 12/11/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PROCEED VENTRAL PATCH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 06/02/2006
Decision Date: 12/11/2006
Regulation Medical Specialty: General & Plastic Surgery