Atlas FDA

Valitude and Visionist Non-MRI CRT-Ps and Valitude X4 and Visionist X4 MRI CRT-Ps

FDA premarket approval P030005/S186 · decided 2019-09-18

Approval details

PMA number
P030005
Supplement
S186
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Valitude and Visionist Non-MRI CRT-Ps and Valitude X4 and Visionist X4 MRI CRT-Ps
Generic name
Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
Applicant
Guidant Corp.
Date received
2019-06-20
Decision date
2019-09-18
Days to decision
90 days
Decision code
APPR
Product code
NKE
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
Approval for hardware modifications to the IS-1 lead bore cavity and spring coil in the IS-1 pulse generator (PG) header for all pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps) within the Accolade family and a subset of implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-D) within the NG3 and NG4 families.

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
FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05 (K061865)Guidant Corp.2006-07-27
HI-TORQUE WHISPER VIEW GUIDE WIRE (K061453)Guidant Corp.2006-06-22
RX ACCUNET 2 EMBOLIC PROTECTION SYSTEM (K042908)Guidant Corp.2004-11-12
ACCUNET EMBOLIC PROTECTION SYSTEM, RX ACCUNET EMBOLIC PROTECTION SYSTEM (K042218)Guidant Corp.2004-08-31
OMNILINK .018 BILIARY STENT SYSTEM (K033834)Guidant Corp.2004-01-02
ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM (K033393)Guidant Corp.2003-11-10
HI-TORQUE BALANCE INIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING (K031678)Guidant Corp.2003-08-26
RAPIDO CUT-AWAY CUTTER (K031459)Guidant Corp.2003-07-23