Safety Alert Summary

Safety Alert Summary

Medical Device Safety Alert: EBI, LLC Biomet SpinalPak Non-invasive Spine Fusion Stimulator System [Part Number: 1067716; UDI-DI: 00812301020218], Biomet OrthoPak Non-invasive Bone Growth Stimulator System [Part Number: 1067718; UD-DI: 00812301020232], 20" Lead Wires, Replacement [Part Number: 1067724-2; UDI-DI: 00812301020300], 48" Lead Wires, Replacement [Part Number: 1067724-4; UDI-DI: 00812301020324]

25 Apr 2024

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=94291

Posted on 25 Apr 2024

Back