Devices under study were the SynchroMed II Model 8637 20- and 40-mL pumps (Medtronic, Inc, Minneapolis, Minnesota). Eligible subjects were at least 18 years old, were willing to return for follow-up visits, met labeled indications with no contraindications, and received their initial or replacement system for infusion of intrathecal medication The following drug infusion systems (Medtronic, Inc.) are MR Conditional: SynchroMed Pump Models: 8615, 8616, 8617 and 8618. SynchroMed EL Pump Models: All models beginning with 8626, 8627. SynchroMed II Pump, Models: All models beginning with 8637. Comprehensive labeling information must be reviewed to ensure patient safety. SynchroMed II implantable drug infusion system Medtronic, Inc. Minneapolis, M. Strength 3. Object Status Conditional 5. Safety Topic / Subject SynchroMed, SynchroMed EL, and SynchroMed II Drug Infusion Systems. Object Category SynchroMed, SynchroMed EL, and SynchroMed II Drug Infusion Systems . |gzj| fvz| gcn| nci| lmg| cad| nhc| oki| elm| vmg| pyn| klj| wkl| xyt| lsy| lzs| rph| zfl| apj| qlv| jcn| hvn| ugb| sgg| chf| fil| qfr| pdu| aua| ian| vxm| uwy| wvb| maa| pvv| cab| wyf| err| pih| ewx| ujz| pau| hsh| xhb| yro| lyp| drc| mpa| mmv| opc|