Atlas FDA

RelayPro Thoracic Stent-Graft System

FDA premarket approval P200045/S014 · decided 2024-11-18

Approval details

PMA number
P200045
Supplement
S014
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
RelayPro Thoracic Stent-Graft System
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Bolton Medical, Inc.
Date received
2024-08-30
Decision date
2024-11-18
Days to decision
80 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Sunrise, FL
Statement
approval for changes to the packaging of the TREO Abdominal Stent Graft System and RelayPro Thoracic Stent Graft System

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510(k) clearances by this applicant

RecordFirmDate
BOLTON PTA CATHETER (K021996)Bolton Medical, Inc.2002-08-23