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AMPLATZER SEPTAL OCCLUDER

FDA premarket approval P000039/S047 · decided 2012-12-19

Approval details

PMA number
P000039
Supplement
S047
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
AMPLATZER SEPTAL OCCLUDER
Generic name
OCCLUDER, PATENT DUCTUS, ARTERIOSUS
Applicant
ABBOTT MEDICAL
Date received
2012-11-30
Decision date
2012-12-19
Days to decision
19 days
Decision code
APPR
Product code
MAE
Advisory committee
Cardiovascular
Expedited review
No
Location
St. Paul, MN
Statement
APPROVAL FOR LABELING CHANGES REGARDING DEVICE EROSION.

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510(k) clearances by this applicant

RecordFirmDate
EnSite™ X EP System (K262006)Abbott Medical2026-07-15
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EnSite™ X EP System (K260212)ABBOTT MEDICAL2026-04-20
Disposable Radiofrequency Cannula (K253907)ABBOTT MEDICAL2026-04-16
Amplatzer™ Trevisio™ Intravascular Delivery System; 9-ATV06F45/609-ATV07F45/609-ATV07F45/809-ATV08F45/609-ATV08F45/809-ATV09F45/809-ATV10F45/809-ATV12F45/80 (K260499)ABBOTT MEDICAL2026-03-13
Armada™ 14 NC PTA Catheter (K252512)ABBOTT MEDICAL2026-02-13
Assert-IQ (DM5100) (K253516)ABBOTT MEDICAL2025-12-18