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FDA 510(k), K072370, SURGICRAFT SURGICAL MESH SYSTEM
FDA 510(k), K072370, SURGICRAFT SURGICAL MESH SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K072370
Device Name: SURGICRAFT SURGICAL MESH SYSTEM
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 08/23/2007
Decision Date: 07/24/2008
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SURGICRAFT SURGICAL MESH SYSTEM
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 08/23/2007
Decision Date: 07/24/2008
Regulation Medical Specialty: General & Plastic Surgery
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