Atlas FDA

Zenith Fenestrated AAA Endovascular Graft

FDA premarket approval P020018/S060 · decided 2022-01-20

Approval details

PMA number
P020018
Supplement
S060
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
Zenith Fenestrated AAA Endovascular Graft
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Cook, Inc.
Date received
2021-07-23
Decision date
2022-01-20
Days to decision
181 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Bloomington, IN
Statement
Approval of the labeling updates for the post-approval study (PAS) protocol.

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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