Premarket Approval (PMA)

Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.

• Device: MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
• Generic Name: Implantable pulse generator, pacemaker (non-CRT)
• Applicant: CARDIAC CONTROL SYSTEMS, INC.; 3 COMMERCE BLVD.; PALM COAST, FL 32164
• PMA Number: P860027
• Date Received: 07/28/1986
• Decision Date: 02/27/1987
• Product Code: LWP
• Docket Number: 87M-0085
• Notice Date: 04/16/1987
• Advisory Committee: Cardiovascular
• Expedited Review Granted?: No
• Combination Product: No
• Supplements: S001 S002 S003 S004 S005 S006 S007 S008 S009 S010 S011 ; S012