Atlas FDA

CentriMag™ Circulatory Support System

FDA premarket approval P170038/S012 · decided 2024-01-09

Approval details

PMA number
P170038
Supplement
S012
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CentriMag™ Circulatory Support System
Generic name
Ventricular (assist) bypass
Applicant
Abbott
Date received
2023-02-23
Decision date
2024-01-09
Days to decision
320 days
Decision code
APPR
Product code
DSQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Pleasanton, CA
Statement
approval for a design change to the CentriMag Motor locking feature.

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
Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter (K261825)Abbott2026-07-02
Amplatzer TorqVue Delivery System (K260993)Abbott2026-04-24
Assert-IQ (DM5000); Assert-IQ (DM5300); Assert-IQ (DM5500); Merlin.net (MN7000) (K251221)Abbott2025-09-17
Lingo Glucose System (K233655)Abbott2024-05-29
CentriMag Pre-connected Pack (K222297)Abbott2022-12-01
EnSite X EP System (K221213)Abbott2022-08-18
EnSite X EP System (K212061)Abbott2021-10-22
WorkMate Claris System (K210392)Abbott2021-03-11