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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K163375
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Product Description
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Recall
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FDA Recall
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INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 24mm, REF 3604024... 2 04/19/2023 Medtronic Sofamor Danek USA Inc
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 26mm, REF 3604026... 2 04/19/2023 Medtronic Sofamor Danek USA Inc
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 32mm, REF 3604532... 2 04/19/2023 Medtronic Sofamor Danek USA Inc
INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 34mm, REF 3604034... 2 04/19/2023 Medtronic Sofamor Danek USA Inc
INFINITY Occipitocervical Upper Thoracic System, PARTIALLY THREADED MULTI AXIAL SCREW, Size: 4.0mm ... 2 04/19/2023 Medtronic Sofamor Danek USA Inc
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