Atlas FDA

DiamondTemp Radiofrequency Generator

FDA premarket approval P200028/S008 · decided 2022-03-17

Approval details

PMA number
P200028
Supplement
S008
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
DiamondTemp Radiofrequency Generator
Generic name
Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
Applicant
Medtronic, Inc.
Date received
2021-12-22
Decision date
2022-03-17
Days to decision
85 days
Decision code
APPR
Product code
OAE
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for software changes to the DiamondTemp Radiofrequency (RF) Generator.

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