K242243
- 510(k) number
- K242243
- Device name
- Target Detachable Coils
- Applicant
- Stryker Neurovscular CA · US
- Product code
- HCG — Device, Neurovascular Embolization
- Decision date
- 2024-08-29
- Date received
- 2024-07-31
- 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: K242243.pdf
Official FDA record: K242243
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.