MAGNA ABUTMENT— 510(k) K984297
Substantially EquivalentFactor, Ii, Inc.
FDA 510(k) clearance K984297 for MAGNA ABUTMENT, Substantially Equivalent on 2000-01-28. Applicant: Factor, Ii, Inc..
Clearance details
- Applicant
- Factor, Ii, Inc.
- Product code
- Code DZE
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lakeside, AZ, US
Adverse events under product code DZE
product code DZE- Death
- 28
- Injury
- 3,367,041
- Malfunction
- 19,958
- Other
- 13
- Total
- 3,387,040
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.