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FDA 510(k), K984220, MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH
FDA 510(k), K984220, MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH
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510(K) Number: K984220
Device Name: MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH
Manufacturer: GREGORY R JONES
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 11/25/1998
Date Received: 02/23/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH
Manufacturer: GREGORY R JONES
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 11/25/1998
Date Received: 02/23/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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