IPS e.max® Press Abutment Solutions for Viteo Base Ti— 510(k) K160798
Substantially EquivalentIvoclar Vivadent, AG
FDA 510(k) clearance K160798 for IPS e.max® Press Abutment Solutions for Viteo Base Ti, Substantially Equivalent on 2016-12-15. Applicant: Ivoclar Vivadent, AG.
Clearance details
- Applicant
- Ivoclar Vivadent, AG
- Product code
- Code NHA
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Schaan, LI
Adverse events under product code NHA
product code NHA- Injury
- 1,270
- Malfunction
- 2,860
- Total
- 4,130
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.