Atlas FDA

Protecta CRT-D and Protecta XT CRT-D

FDA premarket approval P010031/S720 · decided 2020-12-17

Approval details

PMA number
P010031
Supplement
S720
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Protecta CRT-D and Protecta XT CRT-D
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
Medtronic Cardiac Rhythm Disease Management
Date received
2020-10-20
Decision date
2020-12-17
Days to decision
58 days
Decision code
APPR
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for RAMware updates to the Protecta family of devices.

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