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TriClip G4 Delivery System;TriClip G5 Delivery System

FDA premarket approval P230007/S012 · decided 2025-05-18

Approval details

PMA number
P230007
Supplement
S012
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TriClip G4 Delivery System;TriClip G5 Delivery System
Generic name
Tricuspid valve repair device, percutaneously delivered
Applicant
ABBOTT MEDICAL
Date received
2025-04-28
Decision date
2025-05-18
Days to decision
20 days
Decision code
OK30
Product code
NPS
Advisory committee
Cardiovascular
Expedited review
No
Location
St. Paul, MN
Statement
a change in the incoming inspection requirement for functional inspection points for a subassembly component used in the manufacture of the MitraClip and TriClip clip delivery systems (CDS)

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510(k) clearances by this applicant

RecordFirmDate
EnSite™ X EP System (K262006)Abbott Medical2026-07-15
Amplatzer TorqVue Exchange System (K261631)Abbott Medical2026-06-17
OPTIS Mobile Next Imaging System (1014932); OPTIS Integrated Next Imaging System (1014933); Ultreon 3.0 Software Upgrade Kit (ULTR300001) (K253459)ABBOTT MEDICAL2026-04-24
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