FDA 510(k), K962530, PROLENE POLYPROPYLENE MESH NONABSORBABLE SYNTHETIC SURGICAL MESH
FDA 510(k), K962530, PROLENE POLYPROPYLENE MESH NONABSORBABLE SYNTHETIC SURGICAL MESH
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510(K) Number: K962530
Device Name: PROLENE POLYPROPYLENE MESH NONABSORBABLE SYNTHETIC SURGICAL MESH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 06/28/1996
Decision Date: 08/09/1996
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PROLENE POLYPROPYLENE MESH NONABSORBABLE SYNTHETIC SURGICAL MESH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 06/28/1996
Decision Date: 08/09/1996
Regulation Medical Specialty: General & Plastic Surgery