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Zenith® Fenestrated AAA Endovascular Graft, Zenith® Flex AAA Endovascular System

FDA premarket approval P020018/S061 · decided 2023-12-14

Approval details

PMA number
P020018
Supplement
S061
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Zenith® Fenestrated AAA Endovascular Graft, Zenith® Flex AAA Endovascular System
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Cook, Inc.
Date received
2023-11-16
Decision date
2023-12-14
Days to decision
28 days
Decision code
OK30
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Bloomington, IN
Statement
addition of a different form of the inner PTFE liner material used in the Zenith Introduction Systems

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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