Straumann Screw-Retained Abutments— 510(k) K192401
Substantially EquivalentStraumann USA, LLC
FDA 510(k) clearance K192401 for Straumann Screw-Retained Abutments, Substantially Equivalent on 2020-04-06. Applicant: Straumann USA, LLC.
Clearance details
- Applicant
- Straumann USA, LLC
- Product code
- Code NHA
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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.