Atlas FDA

Reply Sr, Reply DR, Esprit SR, Esprit DR Pacemakers

FDA premarket approval P950029/S111 · decided 2016-09-27

Approval details

PMA number
P950029
Supplement
S111
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Reply Sr, Reply DR, Esprit SR, Esprit DR Pacemakers
Generic name
implantable pacemaker Pulse-generator
Applicant
MicroPort CRM USA, Inc.
Date received
2016-07-21
Decision date
2016-09-27
Days to decision
68 days
Decision code
APPR
Product code
DXY
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
Approval for Remote Monitoring System software version 3.7.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.