FDA PMA FDA Class 3 Approved 🇺🇸 United States

Leadless Pacemaker

PMA: P150033 · Supplement: S223 · Decision Apr 30, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0

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Basic Information

Device Name
Leadless Pacemaker
Trade Name
Micra AV TPS (MC1AVR1); Micra AV2 TPS (MC2AVR1); Micra TPS (MC1VR01); Micra VR2 TPS (MC2VR01)
PMA Number
P150033
Supplement Number
S223
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
April 30, 2026
Date Received
January 30, 2026
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for updates to the manufacturing acceptance conditions for plated through holes in hybrid subassemblies incorporated into implantable cardiac rhythm management devices.

Classifications

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

Product Code Device Name
PNJ Leadless Pacemaker