AnatomicAligner— 510(k) K190767
Substantially EquivalentThe Methodist Hospital Research Institute D/B/A Houston
FDA 510(k) clearance K190767 for AnatomicAligner, Substantially Equivalent on 2020-03-16. Applicant: The Methodist Hospital Research Institute D/B/A Houston.
Clearance details
- Applicant
- The Methodist Hospital Research Institute D/B/A Houston
- Product code
- Code LLZ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Adverse events under product code LLZ
product code LLZ- Death
- 13
- Total
- 13
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.