Premarket Approval (PMA)

Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.

• Device: MATRIX VASCULAR CLOSURE SYSTEM (VSG)
• Generic Name: Device, hemostasis, vascular
• Applicant: Cordis US Corporation; 14201 NW 60th Avenue; Miami Lakes, FL 33014
• PMA Number: P040044
• Date Received: 11/04/2004
• Decision Date: 08/17/2005
• Product Code: MGB
• Docket Number: 05M-0359
• Notice Date: 09/08/2005
• Advisory Committee: Cardiovascular
• Expedited Review Granted?: No
• Combination Product: No
• Recalls: CDRH Recalls

Approval Order Statement  
APPROVAL FOR THE MATRIX VSG SYSTEM, MODEL MX-100. THE DEVICE IS INDICATED FOR USE TO SEAL FEMORAL ARTERIAL ACCESS SITES WHILE REDUCING TIMES TO HEMOSTASIS AND AMBULATION IN PATIENTS WHO HAVE UNDERGONE DIAGNOSTIC OR INTERVENTIONAL ENDOVASCULAR PROCEDURES UTILIZING A 5F, 6F, OR 7F PROCEDURAL SHEATH.

• Approval Order: Approval Order
• Summary: Summary of Safety and Effectiveness
• Labeling: Labeling
• Supplements: S001 S002 S003 S004 S005 S006 S007 S008 S009 S010 S011 ; S012 S013 S014 S015 S016 S017 S019 S020 S021 S022 S023 S024 ; S025 S026 S027 S028 S029 S030 S031 S032 S033 S034 S036 S037 ; S038 S039 S040 S041 S042 S043 S044 S045 S046 S047 S048 S049 ; S050 S051 S052 S053 S054 S055 S056 S057 S058 S059 S060 S061 ; S062 S063 S064 S065 S066 S068 S069 S070 S072 S073 S074 S075 ; S076 S077 S078 S079 S080 S081 S082 S083 S084 S085 S086 S087 ; S088 S089 S090 S091 S092 S093 S094 S095 S096 S099 S100 S101