Atlas FDA

CCS MODEL 300 PACEMAKER MAESTRO

FDA premarket approval P890039/S010 · decided 1993-02-12

Approval details

PMA number
P890039
Supplement
S010
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CCS MODEL 300 PACEMAKER MAESTRO
Generic name
implantable pacemaker Pulse-generator
Applicant
Cardiac Control Systems, Inc.
Date received
1992-08-13
Decision date
1993-02-12
Days to decision
183 days
Decision code
APPR
Product code
DXY
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