Atlas FDA

Epic Plus and Epic Plus Supra

FDA premarket approval P040021/S056 · decided 2024-01-23

Approval details

PMA number
P040021
Supplement
S056
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Epic Plus and Epic Plus Supra
Generic name
heart-valve, non-allograft tissue
Applicant
ABBOTT MEDICAL
Date received
2023-11-17
Decision date
2024-01-23
Days to decision
67 days
Decision code
APPR
Product code
LWR
Advisory committee
Cardiovascular
Expedited review
No
Location
St. Paul, MN
Statement
approval for a modification to the stainless steel material used for the annular and post wire components of the Epic Plus and Epic Plus Supra tissue heart valves

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510(k) clearances by this applicant

RecordFirmDate
EnSite™ X EP System (K262006)Abbott Medical2026-07-15
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OPTIS Mobile Next Imaging System (1014932); OPTIS Integrated Next Imaging System (1014933); Ultreon 3.0 Software Upgrade Kit (ULTR300001) (K253459)ABBOTT MEDICAL2026-04-24
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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