MAESTRO(R) SAVVI(TM) SERIES 305 VDD PACING SYSTEM

FDA Premarket Approval P890039 S007

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceMAESTRO(R) SAVVI(TM) SERIES 305 VDD PACING SYSTEM
Generic NameImplantable Pacemaker Pulse-generator
ApplicantCARDIAC CONTROL SYSTEMS, INC.
Date Received1992-06-03
Decision Date1993-04-05
PMAP890039
SupplementS007
Product CodeDXY 
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address CARDIAC CONTROL SYSTEMS, INC. 3 Commerce Blvd. palm Coast, FL 32164

Supplemental Filings

Supplement NumberDateSupplement Type
P890039Original Filing
S016 1996-07-19 Normal 180 Day Track
S015 1995-12-26 Normal 180 Day Track
S014 1995-03-23 Normal 180 Day Track
S013 1994-04-07 Normal 180 Day Track
S012 1993-10-04 Normal 180 Day Track
S011 1993-04-08 Normal 180 Day Track
S010 1992-08-13 Normal 180 Day Track
S009 1992-06-15 Normal 180 Day Track
S008 1992-06-04 Normal 180 Day Track
S007 1992-06-03 Normal 180 Day Track
S006 1992-03-30 Normal 180 Day Track
S005 1991-09-03 Normal 180 Day Track
S004 1991-09-03 Normal 180 Day Track
S003 1991-04-04 Normal 180 Day Track
S002 1991-01-04 Normal 180 Day Track
S001 1990-12-17 Normal 180 Day Track

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