K240651
- 510(k) number
- K240651
- Device name
- MRI Universal
- Applicant
- Stryker Leibinger GmbH & Co KG DE
- Product code
- JEY — Plate, Bone
- Decision date
- 2024-07-12
- Date received
- 2024-03-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K240651.pdf
Official FDA record: K240651
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.