Atlas FDA

Tendril STS, UltiPace

FDA premarket approval P960013/S123 · decided 2023-11-28

Approval details

PMA number
P960013
Supplement
S123
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Tendril STS, UltiPace
Generic name
Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
Applicant
ABBOTT MEDICAL
Date received
2023-08-31
Decision date
2023-11-28
Days to decision
89 days
Decision code
APPR
Product code
NVN
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
the labeling expansion of the currently marketed, Tendril STS (model 2088TC) and UltiPace (LPA1231) leads to include left bundle branch area pacing as an alternative to right ventricular pacing.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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