Atlas FDA

Setrox S 53; Safio S 53; Dextrus 4136;TILDA R53;Solia S 45/53/60, JT 45/53; Siello S53/60/45/53/60/,JT 45/53;

FDA premarket approval P950037/S198 · decided 2019-04-29

Approval details

PMA number
P950037
Supplement
S198
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Setrox S 53; Safio S 53; Dextrus 4136;TILDA R53;Solia S 45/53/60, JT 45/53; Siello S53/60/45/53/60/,JT 45/53;
Generic name
implantable pacemaker Pulse-generator
Applicant
Biotronik, Inc.
Date received
2018-11-01
Decision date
2019-04-29
Days to decision
179 days
Decision code
APPR
Product code
DXY
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
Approval for MR conditional labeling for ProMRI DX systems with a partially capped DX lead.

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510(k) clearances by this applicant

RecordFirmDate
BIOMONITOR IV (471155) (K261074)Biotronik, Inc.2026-05-01
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Pantera Pro; Pantera LEO (K242969)Biotronik, Inc.2024-10-25
Selectra 3D Lead Delivery System (443624-443629, 451789-451791); Selectra Slitter Tool (383119); Selectra Accessory Kit (375518) (K240787)Biotronik, Inc.2024-09-12
Oscar Peripheral Multifunctional Catheter system (K241711)Biotronik, Inc.2024-07-11
BIOMONITOR IV (K230375)Biotronik, Inc.2023-05-19
Passeo-35 Xeo Peripheral Dilatation Catheter (K222065)Biotronik, Inc.2023-02-16
BIOMONITOR IIIm, BIOMONITOR III (K221856)Biotronik, Inc.2022-07-27