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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: K041454
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Product Description
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Recall
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FDA Recall
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Extremities, Large Kit Assy, US, 15/3 - Product Usage: is an injectable, moldable and biocompatible ... 2 06/16/2020 Medtronic Sofamor Danek USA Inc
Medtronic Bone Void Filler, Small - Product Usage: is an injectable, moldable and biocompatible ca... 2 06/16/2020 Medtronic Sofamor Danek USA Inc
Medtronic Bone Void Filler, Large - Product Usage: is an injectable, moldable and biocompatible ca... 2 06/16/2020 Medtronic Sofamor Danek USA Inc
Kyphon brand KyphoPak Express Tray First Fracture, 15/2 with KyphX Osteo Introducer System; Catalog ... 2 09/09/2011 Medtronic Spine LLC (formerly Kyphon Inc.)
KyphX Xpander Inflatable Bone Tamp, size 15/3, Catalog Number K09A, Manufactured by Kyphon Sarl, Swi... 2 05/11/2009 Medtronic Spine LLC, formerly Kyphon Inc
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