K261866
- 510(k) number
- K261866
- Device name
- Concerto Versa Detachable Coil
- Applicant
- Medtronic, Inc. MN · US
- Product code
- KRD — Device, Vascular, For Promoting Embolization
- Decision date
- 2026-06-24
- Date received
- 2026-06-04
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K261866.pdf
Official FDA record: K261866
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.