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FDA 510(k), K002699, PARIETEX COMPOSITE (PCO) MESH
FDA 510(k), K002699, PARIETEX COMPOSITE (PCO) MESH
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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
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
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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