Atlas FDA

Carpentier-Edwards PERIMOUNT Plus Pericardial Mitral Bioprosthesis/Theon Pericardial Mitral Bioprosthesis with ThermaFix

FDA premarket approval P860057/S185 · decided 2018-12-01

Approval details

PMA number
P860057
Supplement
S185
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Carpentier-Edwards PERIMOUNT Plus Pericardial Mitral Bioprosthesis/Theon Pericardial Mitral Bioprosthesis with ThermaFix
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2018-11-07
Decision date
2018-12-01
Days to decision
24 days
Decision code
OK30
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Use of the Carpentier-Edwards PERIMOUNT Model 6900P sewing ring in the Carpentier-Edwards PERIMOUNT Model 6900PTFX valve.

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510(k) clearances by this applicant

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