LOCATOR RTx— 510(k) K150295
Substantially EquivalentZest Anchors, Inc.
FDA 510(k) clearance K150295 for LOCATOR RTx, Substantially Equivalent on 2015-07-24. Applicant: Zest Anchors, Inc..
Clearance details
- Applicant
- Zest Anchors, Inc.
- Product code
- Code NHA
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Escondido, CA, 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.