Atlas FDA

Zenith Fenestrated AAA Endovascular Graft

FDA premarket approval P020018/S063 · decided 2024-04-29

Approval details

PMA number
P020018
Supplement
S063
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Zenith Fenestrated AAA Endovascular Graft
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Cook, Inc.
Date received
2024-04-05
Decision date
2024-04-29
Days to decision
24 days
Decision code
OK30
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Bloomington, IN
Statement
use of an alternative suture in manufacturing of the Zenith® Fenestrated AAA Endovascular Graft, Zenith Alpha™ Thoracic Endovascular Graft, and Zenith® Dissection Endovascular System

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510(k) clearances by this applicant

RecordFirmDate
BEACON TIP TORCON NB ADVANTAGE CATHETER, TORCON NB ADVANTAGE CATHETER (K133130)Cook, Inc.2015-01-09
ADVANCE SALIVARY BALLOON CATHETER WITH WIRE GUIDE (K140593)Cook, Inc.2014-12-15
FLEXOR RADIAL HYDROPHILIC INTRODUCER ACCESS SET (K132592)Cook, Inc.2014-10-09
CIAGLIA PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET/TRAY, CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET/TRAY (K133597)Cook, Inc.2014-04-18
CANTATA(R) 2.9 MICROCATHETER (K131772)Cook, Inc.2014-02-20
ADVANCE CS CORONARY SINUS INFUSION CATHETER (K131204)Cook, Inc.2014-01-29
SPECTRUM TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET (K133634)Cook, Inc.2013-12-23
ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETER (K132020)Cook, Inc.2013-10-25