Implanted electrical device intended for treatment of fecal incontinence
FDA product code QON · Class 3 · 13 devices · 7,602 reports · 1 devices named in recalls
- InterStim™ X 97800Medtronic, Inc. · Implanted electrical device intended for treatment of fecal incontinence5,930 reports
- INTERSTIM® II 3058Medtronic, Inc. · Implanted electrical device intended for treatment of fecal incontinence990 reports
- Axonics 1201Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence481 reports
- NA TH90QFAMedtronic, Inc. · Implanted electrical device intended for treatment of fecal incontinence1 recall0 reports
- InterStim™ Micro SureScan™ MRI 97810Medtronic, Inc. · Implanted electrical device intended for treatment of fecal incontinence50 reports
- Axonics 1701Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence31 reports
- Verify™ 353101Medtronic, Inc. · Implanted electrical device intended for treatment of fecal incontinence29 reports
- Verify® 353101Medtronic, Inc. · Implanted electrical device intended for treatment of fecal incontinence24 reports
- Axonics 1601Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence20 reports
- Axonics 1801Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence18 reports
- Axonics 1901Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence18 reports
- Axonics 2201Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence6 reports
- Axonics 9009Axonics Modulation Technologies, Inc. · Implanted Electrical Device Intended For Treatment Of Fecal Incontinence5 reports