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CELERITY 2D/3D/PILOT STEROID-ELUTING LV LEAD, COROX (-S/-L) BP STEROID-ELUTING LV LEAD

FDA premarket approval P070008/S054 · decided 2014-09-16

Approval details

PMA number
P070008
Supplement
S054
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CELERITY 2D/3D/PILOT STEROID-ELUTING LV LEAD, COROX (-S/-L) BP STEROID-ELUTING LV LEAD
Generic name
Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
Applicant
Biotronik, Inc.
Date received
2014-07-28
Decision date
2014-09-16
Days to decision
50 days
Decision code
APPR
Product code
NKE
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR THE FOLLOWING CHANGES:1) A MINOR MODIFICATION (ADDITION OF INNER COATING) OF TO THE LINOXSMART/ VOLTA/PROTEGOICD LEADS;2) MODIFICATIONS TO THE CURRENT SUTURE SLEEVE TO CREATE A WHITE SUTURE SLEEVE; 3) PA 11 ADAPTER; AND4) LEAD TECHNICAL MANUAL/LABELING UPDATES.

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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
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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