Atlas FDA

KONECT RESILIA Aortic Valved Conduit (AVC)

FDA premarket approval P150048/S083 · decided 2024-11-07

Approval details

PMA number
P150048
Supplement
S083
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
KONECT RESILIA Aortic Valved Conduit (AVC)
Generic name
heart-valve, non-allograft tissue
Applicant
Edwards Lifesciences, LLC
Date received
2024-10-09
Decision date
2024-11-07
Days to decision
29 days
Decision code
OK30
Product code
LWR
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
the use of tissue coupon surrogates in lieu of whole sterilized valves to perform Glycerol Content Lot release testing for KONECT RESILIA AVC devices

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510(k) clearances by this applicant

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Respiration Rate algorithm (K251326)Edwards Lifesciences, LLC2026-06-11
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Edwards MC3 Tricuspid annuloplasty ring (4900) (K251982)Edwards Lifesciences, LLC2025-09-23
Carpentier-Edwards Physio Annuloplasty Ring (4450) (K251688)Edwards Lifesciences, LLC2025-09-17
Hypertension Prediction Index (HePI) Algorithm (K242518)Edwards Lifesciences, LLC2025-05-15
FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors (K242909)Edwards Lifesciences, LLC2025-03-21
Fogarty Thru-Lumen Embolectomy Catheter (K240078)Edwards Lifesciences, LLC2024-08-28
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