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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K150254
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Product Description
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FDA Recall
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RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver 2 10/11/2018 RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Pro... 2 10/20/2016 RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation d... 2 05/26/2016 RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
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