Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K150254 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver | 2 | 10/11/2018 |
FEI # 1000115331 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 |
FEI # 1000115331 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 |
FEI # 1000115331 RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) |
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