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
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