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MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG

FDA premarket approval P860027/S005 · decided 1990-05-22

Approval details

PMA number
P860027
Supplement
S005
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Cardiac Control Systems, Inc.
Date received
1990-04-19
Decision date
1990-05-22
Days to decision
33 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Palm Coast, FL

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510(k) clearances by this applicant

RecordFirmDate
INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610 (K971775)Cardiac Control Systems, Inc.1997-12-29
CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER (K946188)Cardiac Control Systems, Inc.1995-05-15
CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER (K950210)Cardiac Control Systems, Inc.1995-05-03
CCS MAESTRO II SERIES 200 CARDIAC PACEMAKER (K923868)Cardiac Control Systems, Inc.1993-05-14
MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE (K905824)Cardiac Control Systems, Inc.1991-05-16
MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACE (K904941)Cardiac Control Systems, Inc.1991-01-03
MAESTRO PACEMAKER TEST MAGNET (K895110)Cardiac Control Systems, Inc.1989-09-26
MAESTRO(R) SERIES 100/200 SINGLE CHAMBER PACEMAKER (K884023)Cardiac Control Systems, Inc.1988-10-17