Product code QSK

Device name
Hybrid Stent Graft, Thoracic Aortic Lesion Treatment
Medical specialty
Unknown
Device class
3
Review panel
CV
Implant
Y
Life sustaining/supporting
Y
GMP exempt
N
Third party review
N
Summary malfunction reporting
Ineligible
Definition
Repair or replacement of damaged or diseased vessel of the aortic arch and descending thoracic aorta, with or without involvement of ascending aorta, using vascular grafts and/or stent grafts placed during open surgical repair.
Source
FDA openFDA device classification dataset

Related PMA Records

PMADeviceApplicantDecision date
P210006S017Thoraflex™ HybridVascutek, Ltd.2026-04-20
P210006S016Thoraflex™ HybridVascutek, Ltd.2026-01-29
P210006S015Thoraflex™ HybridVascutek, Ltd.2025-10-29
P210006S014Thoraflex™ HybridVascutek, Ltd.2025-10-16
P210006S013Thoraflex™ HybridVascutek, Ltd.2025-07-30
P210006S012Thoraflex HybridVascutek, Ltd.2025-04-09
P210006S010Thoraflex™ HybridVascutek, Ltd.2025-03-28
P210006S011Thoraflex™ HybridVascutek, Ltd.2025-01-27
P210006S009Thoraflex™ HybridVascutek, Ltd.2024-08-01
P210006S007Thoraflex™ HybridVascutek, Ltd.2024-01-11
P210006S005Thoraflex HybridVascutek, Ltd.2023-11-20
P210006S006Thoraflex™ HybridVascutek, Ltd.2023-09-21
P210006S004Thoraflex™ HybridVascutek, Ltd.2023-05-26
P210006S003Thoraflex™ HybridVascutek, Ltd.2022-09-29
P210006S001Thoraflex HybridVascutek, Ltd.2022-08-08
P210006S002Thoraflex HybridVascutek, Ltd.2022-06-16
P210006Thoraflex™ HybridVascutek, Ltd.2022-04-19

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05037881031934Thoraflex™ HybridVASCUTEK LTD2025-09-04
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05037881031842Thoraflex™ HybridVASCUTEK LTD2025-09-04
05037881031835Thoraflex™ HybridVASCUTEK LTD2025-09-04
05037881031828Thoraflex™ HybridVASCUTEK LTD2025-09-04
05037881031811Thoraflex™ HybridVASCUTEK LTD2025-09-04
05037881031804Thoraflex™ HybridVASCUTEK LTD2025-09-04
05037881031798Thoraflex™ HybridVASCUTEK LTD2025-09-04
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05037881031743Thoraflex™ HybridVASCUTEK LTD2025-09-04
05037881031736Thoraflex™ HybridVASCUTEK LTD2025-09-04
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