Patient Specific Planning Solution 3D Bone Models— 510(k) K230540
Substantially EquivalentBiomet Manufacturing Corp
FDA 510(k) clearance K230540 for Patient Specific Planning Solution 3D Bone Models, Substantially Equivalent on 2023-07-25. Applicant: Biomet Manufacturing Corp.
Clearance details
- Applicant
- Biomet Manufacturing Corp
- Product code
- Code LLZ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warsaw, IN, 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.