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.
Device | MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG |
Generic Name | Implantable Pulse Generator, Pacemaker (non-crt) |
Applicant | CARDIAC CONTROL SYSTEMS, INC. |
Date Received | 1990-03-20 |
Decision Date | 1990-03-28 |
PMA | P860027 |
Supplement | S004 |
Product Code | LWP |
Advisory Committee | Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Other Report |
Expedited Review | No |
Combination Product | No |
Applicant Address | CARDIAC CONTROL SYSTEMS, INC. 3 Commerce Blvd. palm Coast, FL 32164 |
Supplement Number | Date | Supplement Type |
---|---|---|
P860027 | Original Filing | |
S012 | 1997-06-12 | Real-time Process |
S011 | 1995-12-26 | Normal 180 Day Track |
S010 | 1995-03-01 | Normal 180 Day Track |
S009 | 1992-07-10 | Normal 180 Day Track |
S008 | 1991-01-04 | Normal 180 Day Track |
S007 | 1990-11-08 | Normal 180 Day Track |
S006 | 1990-11-01 | Normal 180 Day Track |
S005 | 1990-04-19 | Normal 180 Day Track |
S004 | 1990-03-20 | Normal 180 Day Track |
S003 | 1988-09-23 | Normal 180 Day Track |
S002 | 1988-02-17 | Normal 180 Day Track |
S001 | 1987-10-14 | Normal 180 Day Track |