FDA 510(k), K002699, PARIETEX COMPOSITE (PCO) MESH

510(K) Number: K002699
Device Name: PARIETEX COMPOSITE (PCO) MESH
Manufacturer: MEDICAL DEVICE CONSULTANTS, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 08/30/2000
Decision Date: 02/15/2001
Regulation Medical Specialty: General & Plastic Surgery

Total pages: 275

Fully redacted pages: 115

Content pages: 160