PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440— 510(k) K082180
Substantially EquivalentAngelus Industria DE Productos Odontologicos
FDA 510(k) clearance K082180 for PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440, Substantially Equivalent on 2008-12-17. Applicant: Angelus Industria DE Productos Odontologicos. Device class: 2.
Clearance details
- Applicant
- Angelus Industria DE Productos Odontologicos
- Product code
- Code EBI
- Device class
- Class 2
- Regulation
- 21 CFR 872.3760
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code EBI
view allMore clearances from Angelus Industria DE Productos Odontologicos
view allAdverse events under product code EBI
product code EBI- Other
- 1
- Total
- 1
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.