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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: 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.
 
DeviceEXCOR® Apex Cannulae
Generic NameVentricular (assist) bypass
ApplicantBerlin Heart, Inc.
9391 Grogan'S Mill Rd.
Suite A-6
The Woodlands, TX 77380
PMA NumberP160035
Supplement NumberS048
Date Received12/11/2024
Decision Date03/11/2025
Product Code DSQ 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for the addition of an injection molded manufacturing process for the EXCOR cannulae and to change the length of the cannulae velour.
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