Atlas FDA

HEARTMATE XVE LVAS

FDA premarket approval P920014/S019 · decided 2004-06-29

Approval details

PMA number
P920014
Supplement
S019
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
HEARTMATE XVE LVAS
Generic name
Ventricular (assist) bypass
Applicant
Thoratec Corp
Date received
2003-02-07
Decision date
2004-06-29
Days to decision
508 days
Decision code
APPR
Product code
DSQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Pleasanton, CA
Statement
APPROVAL OF THE POST APPROVAL STUDY FOR THE DEVICE.

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
CENTRIMAG PRIMARY CONSOLE (2ND GENERATION); MAG MONITOR (K131179)Thoratec Corp2013-07-18