PMA P040044S068

Device: MYNXGRIP VASCULAR CLOSURE DEVICE (5F, 6F/7F)
Applicant: Cordis US Corporation
PMA number: P040044
Supplement: S068
Product code: MGB
Decision date: 2016-09-06
Classification: Device, Hemostasis, Vascular
Generic name: Device, hemostasis, vascular
Approval order statement: Approval for a manufacturing site located at 9020 Activity Road, Suite D, San Diego, California, 92126 for the sterilization of the Mynx Grip Vascular Closure Device (5F/6F/7F) and Mynx Ace Vascular Closure Device (5F/6F/7F).

Current openFDA PMA Record#

Device: MYNXGRIP VASCULAR CLOSURE DEVICE (5F, 6F/7F)
Applicant: Cordis US Corporation
PMA number: P040044
Supplement: S068
Product code: MGB
Generic name: Device, hemostasis, vascular
Decision date: 2016-09-06
Decision code: APPR
Date received: 2015-12-07
Supplement type: Normal 180 Day Track No User Fee
Supplement reason: Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement: Approval for a manufacturing site located at 9020 Activity Road, Suite D, San Diego, California, 92126 for the sterilization of the Mynx Grip Vascular Closure Device (5F/6F/7F) and Mynx Ace Vascular Closure Device (5F/6F/7F).