K230130
- 510(k) number
- K230130
- Device name
- Micromate Navi+
- Applicant
- Isys Medizintechnik GmbH AT
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2023-10-10
- Date received
- 2023-01-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K230130.pdf
Official FDA record: K230130
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.