Device, neurosurgical fragmentation and aspiration
FDA product code LBK · Class U · 10 devices · 63 reports · 1 devices named in recalls
- CUSA® Excel C2600Integra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration1 recall44 reports
- CUSA® Excel C3601Integra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration7 reports
- CUSA® Excel C2601Integra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration3 reports
- CUSA® Excel C3600Integra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration2 reports
- CUSA® Excel CUSAEXCEL2Integra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration2 reports
- CUSA® Excel C4617SIntegra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration1 report
- CUSA® Clarity C7401SIntegra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration1 report
- CUSA® Clarity C7420SIntegra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration1 report
- CUSA® Clarity C7523Integra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration1 report
- CUSA® Clarity C7601EAIntegra Lifesciences (Ireland) Limited · Device, neurosurgical fragmentation and aspiration1 report