Atlas FDA

PERCLOSE PROGLIDE AND PERCLOSE AT 6F SUTURE MEDIATED CLOSURE SYSTEMS

FDA premarket approval P960043/S085 · decided 2014-01-29

Approval details

PMA number
P960043
Supplement
S085
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PERCLOSE PROGLIDE AND PERCLOSE AT 6F SUTURE MEDIATED CLOSURE SYSTEMS
Generic name
Device, hemostasis, vascular
Applicant
Abbott Vascular, Inc.
Date received
2013-12-31
Decision date
2014-01-29
Days to decision
29 days
Decision code
OK30
Product code
MGB
Advisory committee
Cardiovascular
Expedited review
No
Location
Redwood, CA
Statement
CHANGE TO THE JOINT TENSILE TESTING PROCESS.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Hi-Torque JET Guide Wire Family (K142415)Abbott Vascular, Inc.2014-12-19
PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILY (K123067)Abbott Vascular, Inc.2013-01-29
HI-TORQUE COMMAND GUIDE WIRE FAMILY (K122573)Abbott Vascular, Inc.2012-11-20
ARMADA 14 PTA CATHETER (K102705)Abbott Vascular, Inc.2010-12-07
HI-TORQUE WINN GUIDE WIRE FAMILY (K101648)Abbott Vascular, Inc.2010-07-08
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL (K101011)Abbott Vascular, Inc.2010-05-24
HI-TORQUE PROGRESS GUIDE WIRE FAMILY (K091825)Abbott Vascular, Inc.2009-09-25
FOXCROSS PTA CATHETER (K081417)Abbott Vascular, Inc.2008-06-04