Atlas FDA

VALITUDE CRT-P

FDA premarket approval P030005/S144 · decided 2016-11-03

Approval details

PMA number
P030005
Supplement
S144
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VALITUDE CRT-P
Generic name
Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
Applicant
Guidant Corp.
Date received
2016-10-03
Decision date
2016-11-03
Days to decision
31 days
Decision code
OK30
Product code
NKE
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
Additional supplier for the raw material used in low voltage battery lids.

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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