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FDA 510(k) K002699, PARIETEX COMPOSITE (PCO) MESH, by Medical Device Consultants, Inc.

FDA 510(k) K002699, PARIETEX COMPOSITE (PCO) MESH, by Medical Device Consultants, Inc.

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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
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