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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K153530
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Spectranetics Bridge Occlusion Balloon catheter, Sheath Compatibility 12F, Guidewire Compatibility 0... 1 08/26/2017 FEI # 3007284006
Spectranetics Corporation
Bridge Occlusion Balloon, REF 590-001, QTY 1, Sheath Compatibility 12F, Guidewire Compatibility 0.03... 2 06/01/2020 FEI # 3007284006
Spectranetics Corporation
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