FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Leadless Pacemaker

PMA: P150033 · Supplement: S056 · Decision Sep 27, 2019
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
Leadless Pacemaker
Trade Name
Micra TPS
PMA Number
P150033
Supplement Number
S056
Device Class
FDA Class 3
Product Code
PNJ
Generic Name
Leadless pacemaker
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
September 27, 2019
Date Received
September 16, 2019
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Transfer of receiving and incoming inspection activities from Medtronic Rice Creek facility to the Medtronic Puerto Rico Operations Company (MPROC) Villalba, MPROC Juncos, and the Federal Express/Third Party Logistics facility in Guaynabo, Puerto Rico.

Classifications

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

Product Code Device Name
PNJ Leadless Pacemaker