K241895
- 510(k) number
- K241895
- Device name
- Cannulated PsiFGuard
- Applicant
- Spineguard FR
- Product code
- SCY — Sacroiliac Joint Guidewire Placement Device
- Decision date
- 2024-09-26
- Date received
- 2024-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K241895.pdf
Official FDA record: K241895
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.