K261772
- 510(k) number
- K261772
- Device name
- Target Xtra Detachable Coil
- Applicant
- Stryker Neurovscular CA · US
- Product code
- HCG — Device, Neurovascular Embolization
- Decision date
- 2026-06-24
- Date received
- 2026-05-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K261772.pdf
Official FDA record: K261772
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.