PARIETEX COMPOSITE (PCO) MESH


Device Classification Name

mesh, surgical, polymeric

510(k) Number K002699
Device Name PARIETEX COMPOSITE (PCO) MESH
Original Applicant
MEDICAL DEVICE CONSULTANTS, INC.
49 plain st.
north attleboro, 
MA 
02760 -4153

Original Contact mary mcnamara-cullinane
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 08/30/2000
Decision Date 02/15/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No