CARDIAC RESYNCHRONIZATION THERAPY PACEMAKER (CRT-P) DEVICES

FDA premarket approval P010015/S205 · decided 2014-04-10

Approval details

PMA number

P010015

Supplement

S205

Supplement type

Panel Track

Supplement reason

Labeling Change - Indications/instructions/shelf life/tradename

Trade name

CARDIAC RESYNCHRONIZATION THERAPY PACEMAKER (CRT-P) DEVICES

Generic name

Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)

Applicant

Medtronic, Inc.

Date received

2013-05-29

Decision date

2014-04-10

Days to decision

316 days

Decision code

APPR

Product code

NKE

Advisory committee

Cardiovascular

Expedited review

Yes

Location

Mounds View, MN

Statement

APPROVAL FOR THE EXPANSION OF THE INDICATIONS FOR USE OF THE CRT-P AND CRT-D DEVICES TO INCLUDE NYHA FUNCTIONAL CLASS I, II, OR III PATIENTS WHO HAVE A LEFT VENTRICULAR EJECTION FRACTION (LVEF) => 50% ARE ON STABLE, OPTIMAL HEART FAILURE MEDICAL THERAPY IF INDICATED, AND HAVE ATRIOVENTRICULAR BLOCK (AV BLOCK) THAT IS EXPECTED TO REQUIRE A HIGH PERCENTAGE OF VENTRICULAR PACING THAT CANNOT BE MANAGED WITH ALGORITHMS TO MINIMIZE RIGHT VENTRICULAR PACING. THESE DEVICES ARE INDICATED FOR THE FOLLOWIN

510(k) clearances by this applicant