FDA PMA FDA Class 3 Approved 🇺🇸 United States

Leadless Pacemaker

PMA: P150033 · Supplement: S070 · Decision Jun 17, 2020
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
Leadless Pacemaker
Trade Name
Micra Transcatheter Pacing System
PMA Number
P150033
Supplement Number
S070
Device Class
FDA Class 3
Product Code
PNJ
Generic Name
Leadless pacemaker
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 17, 2020
Date Received
April 6, 2020
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol
Expedited Review
N

Advisory Committee Statement

Approval to pool existing usable M-PREP treadmill test data from the Micra IDE, China IDE, and the Micra rate response study.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PNJ Leadless Pacemaker