DYNAMESH -CICAT— 510(k) K131530
Substantially EquivalentFeg Textiltechnik Forschungs-Und Entwicklungsgesel
FDA 510(k) clearance K131530 for DYNAMESH -CICAT, Substantially Equivalent on 2013-10-23. Applicant: Feg Textiltechnik Forschungs-Und Entwicklungsgesel.
Clearance details
- Applicant
- Feg Textiltechnik Forschungs-Und Entwicklungsgesel
- Product code
- Code FTL
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Peterborough, GB
Adverse events under product code FTL
product code FTL- Death
- 317
- Injury
- 66,072
- Malfunction
- 1,273
- Other
- 3
- Total
- 67,665
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.