Atlas FDA

Zenith AAA Endovascular Graft

FDA premarket approval P020018/S058 · decided 2018-07-20

Approval details

PMA number
P020018
Supplement
S058
Supplement type
Special (Immediate Track)
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Zenith AAA Endovascular Graft
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Cook, Inc.
Date received
2018-06-22
Decision date
2018-07-20
Days to decision
28 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Bloomington, IN
Statement
Approval for modifications to the manufacturing instructions for the delivery systems for the Zenith AAA Endovascular Graft.

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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