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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K233318
 
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AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553640 2 01/29/2025 Boston Scientific Corporation
AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553650 2 01/29/2025 Boston Scientific Corporation
AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553660 2 01/29/2025 Boston Scientific Corporation
AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553670 2 01/29/2025 Boston Scientific Corporation
AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553680 2 01/29/2025 Boston Scientific Corporation
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553570 2 01/29/2025 Boston Scientific Corporation
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553520 2 01/29/2025 Boston Scientific Corporation
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553530 2 01/29/2025 Boston Scientific Corporation
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553540 2 01/29/2025 Boston Scientific Corporation
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553550 2 01/29/2025 Boston Scientific Corporation
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