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Hybrid Stent Graft, Thoracic Aortic Lesion Treatment
FDA product code QSK · Class 3 · Unknown
126
Registered devices
323
Adverse events
0
Recalls
0
510(k) clearances
Devices with this code
Thoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTDThoraflex™ Hybrid — VASCUTEK LTD
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