Atlas FDA

Barostim System

FDA premarket approval P180050/S006 · decided 2022-06-14

Approval details

PMA number
P180050
Supplement
S006
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Barostim System
Generic name
Stimulator, carotid sinus nerve
Applicant
Cvrx, Inc.
Date received
2022-05-20
Decision date
2022-06-14
Days to decision
25 days
Decision code
APPR
Product code
DSR
Advisory committee
Cardiovascular
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for the revised statistical analysis plan.

Class III intelligence, same tools

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