FDA 510(k), K001122, PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH
FDA 510(k), K001122, PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH
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510(K) Number: K001122
Device Name: PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 04/07/2000
Decision Date: 05/23/2000
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 04/07/2000
Decision Date: 05/23/2000
Regulation Medical Specialty: General & Plastic Surgery