K890233
Substantially EquivalentSUTURE CLIP APPLIER/REMOVER
- Applicant
- Kinetic Medical Products
- Product code
- GDO
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Erie, PA, US
Adverse events under product code GDO
product code GDO- Death
- 5
- Malfunction
- 2,124
- Total
- 2,129
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.