Atlas FDA

Attain StarFix Lead

FDA premarket approval P060039/S101 · decided 2020-08-06

Approval details

PMA number
P060039
Supplement
S101
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Attain StarFix Lead
Generic name
Drug eluting permanent left ventricular (lv) pacemaker electrode
Applicant
Medtronic, Inc.
Date received
2020-07-09
Decision date
2020-08-06
Days to decision
28 days
Decision code
OK30
Product code
OJX
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Transfer and expand inspection activities at the MPROC Juncos Facility.

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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