Atlas FDA

SYNCRA CRT-P/CONSULTA CRT-P

FDA premarket approval P010015/S113 · decided 2011-05-05

Approval details

PMA number
P010015
Supplement
S113
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SYNCRA CRT-P/CONSULTA CRT-P
Generic name
Drug eluting permanent left ventricular (lv) pacemaker electrode
Applicant
Medtronic, Inc.
Date received
2011-04-04
Decision date
2011-05-05
Days to decision
31 days
Decision code
OK30
Product code
OJX
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
THE SUBJECT DEVICES ARE ABLE TO BE MANUFACTURED USING NEW PLATING LINES AT THE QUALIFIED SUPPLIER.

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
VitalFlow Set with Balance™ Biosurface (K261335)Medtronic, Inc.2026-07-31
Concerto Versa™ Detachable Coil (K261866)Medtronic, Inc.2026-06-24
Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae (K260195)Medtronic, Inc.2026-04-23
Retrograde Coronary Sinus Perfusion Cannulae (K253203)Medtronic, Inc.2026-02-19
Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
Bio-Medicus Life Support Catheter and Introducer (K251831)Medtronic, Inc.2026-01-15
Concerto Versa™ Detachable Coil (K253511)Medtronic, Inc.2026-01-14
C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19