Atlas FDA

Relay Thoracic Stent-Graft With Plus Delivery System

FDA premarket approval P110038/S022 · decided 2019-05-31

Approval details

PMA number
P110038
Supplement
S022
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Relay Thoracic Stent-Graft With Plus Delivery System
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Bolton Medical, Inc.
Date received
2018-12-03
Decision date
2019-05-31
Days to decision
179 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Sunrise, FL
Statement
approval for a sterilization site, Sterigenics U.S. LLC, located at 1148 Porter Avenue, Haw River, North Carolina 27258, as a new gamma sterilization site for the RelayPlus Thoracic Stent Graft System.

Class III intelligence, same tools

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

510(k) clearances by this applicant

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