Atlas FDA

IFORIA/ILESTO/INVENTRA/IPERIA/ITREVIA 5/7 DR-T/VR-T/VR-T DX, & VARIOUS LUMAX ICDS; IFORIA/ILESTO/IPERIA/ITREVIA 5/7 HF-T

FDA premarket approval P050023/S083 · decided 2015-04-09

Approval details

PMA number
P050023
Supplement
S083
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
IFORIA/ILESTO/INVENTRA/IPERIA/ITREVIA 5/7 DR-T/VR-T/VR-T DX, & VARIOUS LUMAX ICDS; IFORIA/ILESTO/IPERIA/ITREVIA 5/7 HF-T
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Applicant
Biotronik, Inc.
Date received
2015-02-13
Decision date
2015-04-09
Days to decision
55 days
Decision code
APPR
Product code
MRM
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR UPDATES TO YOUR ICS 3000/RENAMIC PROGRAMMERSOFTWARE (1501.U).

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510(k) clearances by this applicant

RecordFirmDate
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